UA61895C2 - A method for preparing 1,1,1,3,3-pentafluoropropane - Google Patents

A method for preparing 1,1,1,3,3-pentafluoropropane Download PDF

Info

Publication number: UA61895C2
Authority: UA; Ukraine
Prior art keywords: catalyst; pentachloropropane; item; items; telomerization
Prior art date: 1995-10-23

Application number

UA98042033A

Other languages

English (en)

Ukrainian (uk)

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-10-23

Filing date

1996-04-10

Publication date

2003-12-15

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9483881&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UA61895(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1996-04-10 Application filed filed Critical

2003-12-15 Publication of UA61895C2 publication Critical patent/UA61895C2/uk

Links

MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 title claims abstract description 16
238000000034 method Methods 0.000 title claims description 40
239000003054 catalyst Substances 0.000 claims abstract description 44
VVWFZKBKXPXGBH-UHFFFAOYSA-N 1,1,1,3,3-pentachloropropane Chemical compound ClC(Cl)CC(Cl)(Cl)Cl VVWFZKBKXPXGBH-UHFFFAOYSA-N 0.000 claims abstract description 25
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims abstract description 13
229910000040 hydrogen fluoride Inorganic materials 0.000 claims abstract description 13
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 18
238000006243 chemical reaction Methods 0.000 claims description 16
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 14
229950005499 carbon tetrachloride Drugs 0.000 claims description 13
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 12
229910052751 metal Inorganic materials 0.000 claims description 10
239000002184 metal Substances 0.000 claims description 10
230000000737 periodic effect Effects 0.000 claims description 10
ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical group Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 9
150000002739 metals Chemical class 0.000 claims description 9
150000001805 chlorine compounds Chemical class 0.000 claims description 6
230000003993 interaction Effects 0.000 claims description 6
239000000203 mixture Substances 0.000 claims description 6
150000002825 nitriles Chemical group 0.000 claims description 6
239000002904 solvent Substances 0.000 claims description 6
OHZZTXYKLXZFSZ-UHFFFAOYSA-I manganese(3+) 5,10,15-tris(1-methylpyridin-1-ium-4-yl)-20-(1-methylpyridin-4-ylidene)porphyrin-22-ide pentachloride Chemical compound [Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Mn+3].C1=CN(C)C=CC1=C1C(C=C2)=NC2=C(C=2C=C[N+](C)=CC=2)C([N-]2)=CC=C2C(C=2C=C[N+](C)=CC=2)=C(C=C2)N=C2C(C=2C=C[N+](C)=CC=2)=C2N=C1C=C2 OHZZTXYKLXZFSZ-UHFFFAOYSA-I 0.000 claims description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 4
OMRRUNXAWXNVFW-UHFFFAOYSA-N fluoridochlorine Chemical class ClF OMRRUNXAWXNVFW-UHFFFAOYSA-N 0.000 claims description 4
150000002222 fluorine compounds Chemical class 0.000 claims description 4
229910052718 tin Inorganic materials 0.000 claims description 3
239000005749 Copper compound Substances 0.000 claims description 2
150000001880 copper compounds Chemical class 0.000 claims description 2
229910052742 iron Inorganic materials 0.000 claims description 2
150000002736 metal compounds Chemical class 0.000 claims description 2
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 claims description 2
238000012876 topography Methods 0.000 claims 1
239000012429 reaction media Substances 0.000 description 7
239000007791 liquid phase Substances 0.000 description 6
238000002360 preparation method Methods 0.000 description 4
BBEAZDGZMVABIC-UHFFFAOYSA-N 1,1,1,3,3,3-hexachloropropane Chemical compound ClC(Cl)(Cl)CC(Cl)(Cl)Cl BBEAZDGZMVABIC-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
238000003682 fluorination reaction Methods 0.000 description 3
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
229910000041 hydrogen chloride Inorganic materials 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
239000003426 co-catalyst Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
230000033001 locomotion Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000000523 sample Substances 0.000 description 2
QAERDLQYXMEHEB-UHFFFAOYSA-N 1,1,3,3,3-pentafluoroprop-1-ene Chemical compound FC(F)=CC(F)(F)F QAERDLQYXMEHEB-UHFFFAOYSA-N 0.000 description 1
XAHBEACGJQDUPF-UHFFFAOYSA-N 1,2-dichloro-1,1,3,3,3-pentafluoropropane Chemical compound FC(F)(F)C(Cl)C(F)(F)Cl XAHBEACGJQDUPF-UHFFFAOYSA-N 0.000 description 1
SKDFWEPBABSFMG-UHFFFAOYSA-N 1,2-dichloro-1,1-difluoroethane Chemical compound FC(F)(Cl)CCl SKDFWEPBABSFMG-UHFFFAOYSA-N 0.000 description 1
UHMWWIKRVZTBBR-UHFFFAOYSA-N 1-chloro-1,1,2,2,3-pentafluoropropane Chemical compound FCC(F)(F)C(F)(F)Cl UHMWWIKRVZTBBR-UHFFFAOYSA-N 0.000 description 1
LLJWABOOFANACB-UHFFFAOYSA-N 1-chloro-1,1,3,3,3-pentafluoropropane Chemical compound FC(F)(F)CC(F)(F)Cl LLJWABOOFANACB-UHFFFAOYSA-N 0.000 description 1
OPLWDQVQIWKMSG-UHFFFAOYSA-N 1-chloro-1-fluoropropane Chemical class CCC(F)Cl OPLWDQVQIWKMSG-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
238000011437 continuous method Methods 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002169 ethanolamines Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
-1 for example Chemical class 0.000 description 1
239000007792 gaseous phase Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
230000009545 invasion Effects 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
229910001510 metal chloride Inorganic materials 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229910052715 tantalum Inorganic materials 0.000 description 1
GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
150000003608 titanium Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
- C07C17/206—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being HX
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
- C07C17/278—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of only halogenated hydrocarbons
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

UA98042033A 1995-10-23 1996-04-10 A method for preparing 1,1,1,3,3-pentafluoropropane UA61895C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR9512558A FR2740132B1 (fr)	1995-10-23	1995-10-23	Procede pour la preparation de 1,1,1,3,3-pentafluoropropane
PCT/EP1996/004315 WO1997015540A1 (fr)	1995-10-23	1996-10-04	Procede pour la preparation de 1,1,1,3,3-pentafluoropropane

Publications (1)

Publication Number	Publication Date
UA61895C2 true UA61895C2 (en)	2003-12-15

Family

ID=9483881

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA98042033A UA61895C2 (en)	1995-10-23	1996-04-10	A method for preparing 1,1,1,3,3-pentafluoropropane

Country Status (28)

Country	Link
US (3)	US6730817B1 (de)
EP (1)	EP0858440B1 (de)
JP (3)	JP2000513705A (de)
KR (1)	KR19990066942A (de)
CN (1)	CN1079787C (de)
AR (1)	AR004079A1 (de)
AT (1)	ATE211723T1 (de)
AU (1)	AU722645B2 (de)
BR (1)	BR9611223A (de)
CA (1)	CA2232421C (de)
CZ (1)	CZ291762B6 (de)
DE (1)	DE69618476T2 (de)
DK (1)	DK0858440T3 (de)
EA (1)	EA001416B1 (de)
ES (1)	ES2171228T3 (de)
FR (1)	FR2740132B1 (de)
HU (1)	HU222560B1 (de)
IL (1)	IL124086A (de)
MX (1)	MX9803175A (de)
NO (1)	NO309716B1 (de)
NZ (1)	NZ320161A (de)
PL (1)	PL186534B1 (de)
PT (1)	PT858440E (de)
RO (1)	RO120193B1 (de)
SK (1)	SK282636B6 (de)
UA (1)	UA61895C2 (de)
WO (1)	WO1997015540A1 (de)
ZA (1)	ZA968481B (de)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
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FR2740132B1 (fr) *	1995-10-23	1997-12-19	Solvay	Procede pour la preparation de 1,1,1,3,3-pentafluoropropane
FR2748473B1 (fr) *	1996-05-13	1998-07-24	Atochem Elf Sa	Synthese du 1-chloro-3,3,3 trifluoropropene et sa fluoration en 1,1,1,3,3 pentafluoropropane
US6023004A (en) *	1996-11-12	2000-02-08	Alliedsignal, Inc.	Liquid phase catalytic fluorination of hydrochlorocarbon and hydrochlorofluorocarbon
BE1011319A3 (fr)	1997-05-05	1999-07-06	Solvay	Procede de preparation d'hydrocarbures halogenes.
AU743129B2 (en)	1997-05-05	2002-01-17	Solvay (Societe Anonyme)	Method for preparing 1,1,1,3,3-pentachlorobutane
KR100552273B1 (ko) *	1997-05-05	2006-02-20	솔베이(소시에떼아노님)	할로탄화수소의 제조방법
BE1011188A3 (fr) *	1997-06-02	1999-06-01	Solvay	Procede de preparation d'hydrocarbures halogenes.
BE1011249A3 (fr) *	1997-07-03	1999-06-01	Solvay	Pentachlorobutane, son procede de fabrication et son utilisation, procede de preparation du 1,1-difluoro-2-trifluoromethylpropane et utilisation de ce compose.
JP2001513519A (ja)	1997-08-08	2001-09-04	ソルヴェイ	ハロ炭化水素の製造方法
FR2768726A1 (fr) *	1997-09-23	1999-03-26	Atochem Elf Sa	Synthese du 1, 1, 1, 3, 3-pentafluoropropane
FR2768727A1 (fr) *	1997-09-23	1999-03-26	Atochem Elf Sa	Synthese du 1,1,1,3,3-pentafluoropropane
FR2768717B1 (fr)	1997-09-24	1999-11-12	Solvay	Procede de separation de fluorure d'hydrogene de ses melanges avec un hydrofluoroalcane contenant de 3 a 6 atomes de carbone
BE1012268A3 (fr)	1998-11-05	2000-08-01	Solvay	Procede de preparation d'hydrocarbures halogenes.
RU2261856C2 (ru)	1998-12-18	2005-10-10	Солвей (Сосьете Аноним)	Способ разделения смеси, содержащей по меньшей мере один гидрофторалкан и фтористый водород, способ получения гидрофторалкана и азеотропная композиция
DE60041346D1 (de)	1999-10-06	2009-02-26	Solvay	Verfahren zur herstellung von halogenierten kohlenwasserstoffen in gegenwart eines cokatalysators
CN100467093C (zh)	2001-06-01	2009-03-11	霍尼韦尔国际公司	1,1,1,3,3-五氟丁烷与氟化氢的类共沸组合物
US6500995B1 (en)	2001-06-14	2002-12-31	Vulcan Chemicals	Water-enhanced production of 1,1,1,3,3,-pentachloropropane
US20040249225A1 (en) *	2001-10-24	2004-12-09	Tatsuya Hirata	Method an system for recovery of catalysts and process and unit for production of perfluoroalkyl iodide telomers
US7214839B2 (en) *	2003-05-23	2007-05-08	Honeywell International Inc.	Method of making hydrofluorocarbons
US7371363B2 (en) *	2003-07-15	2008-05-13	Honeywell International Inc.	Methods of purifying hydrogen fluoride
US8645709B2 (en) *	2006-11-14	2014-02-04	Cfph, Llc	Biometric access data encryption
WO2010055146A2 (en) *	2008-11-13	2010-05-20	Solvay Fluor Gmbh	Hydrofluoroolefins, manufacture of hydrofluoroolefins and methods of using hydrofluoroolefins
US8609907B2 (en) *	2008-11-25	2013-12-17	Solvay Fluor Gmbh	Process for the preparation of chlorofluoroalkenes
CN102491871B (zh) *	2011-12-12	2013-12-18	南京信息工程大学	一种七氟丙烷的制备方法
US9353029B2 (en)	2013-03-14	2016-05-31	Honeywell International, Inc.	Fluorination process and reactor
CN104230649A (zh) *	2013-06-18	2014-12-24	林卫荃	五氯丙烷制备方法
JP2017509606A (ja) *	2014-02-19	2017-04-06	アーケマ・インコーポレイテッド	ヒドロクロロフルオロオレフィンを製造するためのプロセス
WO2018237142A1 (en)	2017-06-22	2018-12-27	Westfahl Erick	PORTABLE CLOSURE SYSTEM

Family Cites Families (15)

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Publication number	Priority date	Publication date	Assignee	Title
US3862978A (en) *	1967-08-24	1975-01-28	Dow Chemical Co	Catalytic synthesis of organic halogen compounds from an ethylenically unsaturated compound and a halogenated organic compound
BE1005096A3 (fr) *	1991-07-10	1993-04-20	Solvay	Procede pour la preparation de 1-chloro-1,1,3,3,3-pentafluoropropane et de 1,1,1,3,3,3-hexafluoropropane.
DE4305164A1 (de)	1993-02-19	1994-08-25	Bayer Ag	Verfahren zur Herstellung von 1,1,1,3,3-Pentafluorpropan
US5395997A (en) *	1993-07-29	1995-03-07	Alliedsignal Inc.	Process for the preparation of hydrofluorocarbons having 3 to 7 carbon atoms
WO1995004022A1 (en)	1993-07-29	1995-02-09	Alliedsignal Inc.	Process for the preparation of 1,1,1,3,3-pentafluoropropane
AU7559194A (en)	1993-08-16	1995-03-14	Allied-Signal Inc.	Process for combining chlorine-containing molecules to synthesize fluorine-containing products
JP2818035B2 (ja)	1994-07-11	1998-10-30	アライドシグナル・インコーポレーテッド	１，１，１，３，３−ペンタフルオロプロパンの製造法
FR2724928B1 (fr)	1994-09-26	1996-10-31	Atochem Elf Sa	Synthese de 1,1,1,3,3-pentafluoropropane
EP0729932A1 (de) *	1995-03-03	1996-09-04	Central Glass Company, Limited	Verfahren zur Herstellung von Halopropan
JPH08239334A (ja) *	1995-03-03	1996-09-17	Central Glass Co Ltd	１，１，１，３，３−ペンタフルオロプロパンの製造方法
JP3414562B2 (ja) *	1995-10-13	2003-06-09	ダイキン工業株式会社	１，１，１，３，３−ペンタフルオロプロパンの製造方法
FR2740132B1 (fr) *	1995-10-23	1997-12-19	Solvay	Procede pour la preparation de 1,1,1,3,3-pentafluoropropane
JPH09268141A (ja) *	1996-04-03	1997-10-14	Central Glass Co Ltd	１，１，１，３，３−ペンタフルオロプロパンの製造方法
JP3831987B2 (ja) *	1996-09-25	2006-10-11	旭硝子株式会社	１，１，１，３，３−ペンタフルオロプロパンの製造方法
JPH10101594A (ja) *	1996-09-25	1998-04-21	Asahi Glass Co Ltd	１，１，１，３，３−ペンタフルオロプロパンの製造法

1995
- 1995-10-23 FR FR9512558A patent/FR2740132B1/fr not_active Expired - Lifetime
1996
- 1996-04-10 UA UA98042033A patent/UA61895C2/uk unknown
- 1996-10-04 NZ NZ320161A patent/NZ320161A/xx not_active IP Right Cessation
- 1996-10-04 EP EP96934532A patent/EP0858440B1/de not_active Expired - Lifetime
- 1996-10-04 IL IL12408696A patent/IL124086A/xx not_active IP Right Cessation
- 1996-10-04 HU HU9802978A patent/HU222560B1/hu active IP Right Grant
- 1996-10-04 DK DK96934532T patent/DK0858440T3/da active
- 1996-10-04 PT PT96934532T patent/PT858440E/pt unknown
- 1996-10-04 BR BR9611223A patent/BR9611223A/pt not_active IP Right Cessation
- 1996-10-04 CN CN96199236A patent/CN1079787C/zh not_active Expired - Lifetime
- 1996-10-04 AU AU72849/96A patent/AU722645B2/en not_active Expired
- 1996-10-04 CA CA002232421A patent/CA2232421C/fr not_active Expired - Lifetime
- 1996-10-04 WO PCT/EP1996/004315 patent/WO1997015540A1/fr active Search and Examination
- 1996-10-04 AT AT96934532T patent/ATE211723T1/de active
- 1996-10-04 SK SK489-98A patent/SK282636B6/sk not_active IP Right Cessation
- 1996-10-04 CZ CZ19981254A patent/CZ291762B6/cs not_active IP Right Cessation
- 1996-10-04 RO RO98-00880A patent/RO120193B1/ro unknown
- 1996-10-04 EA EA199800322A patent/EA001416B1/ru not_active IP Right Cessation
- 1996-10-04 US US09/051,746 patent/US6730817B1/en not_active Expired - Fee Related
- 1996-10-04 ES ES96934532T patent/ES2171228T3/es not_active Expired - Lifetime
- 1996-10-04 KR KR1019980702865A patent/KR19990066942A/ko not_active Application Discontinuation
- 1996-10-04 DE DE69618476T patent/DE69618476T2/de not_active Expired - Lifetime
- 1996-10-04 JP JP09516231A patent/JP2000513705A/ja active Pending
- 1996-10-04 PL PL96326367A patent/PL186534B1/pl unknown
- 1996-10-08 ZA ZA968481A patent/ZA968481B/xx unknown
- 1996-10-23 AR ARP960104867A patent/AR004079A1/es active IP Right Grant
1998
- 1998-04-22 NO NO981800A patent/NO309716B1/no not_active IP Right Cessation
- 1998-04-23 MX MX9803175A patent/MX9803175A/es unknown
2003
- 2003-07-03 US US10/613,546 patent/US6930215B2/en not_active Expired - Fee Related
2005
- 2005-07-19 US US11/184,353 patent/US20050256348A1/en not_active Abandoned
2007
- 2007-06-12 JP JP2007154930A patent/JP2007262084A/ja active Pending
2008
- 2008-11-13 JP JP2008291297A patent/JP2009084290A/ja active Pending

Also Published As

Publication number	Publication date
SK48998A3 (en)	1998-09-09
CN1079787C (zh)	2002-02-27
HUP9802978A3 (en)	2000-07-28
US6730817B1 (en)	2004-05-04
CN1205682A (zh)	1999-01-20
JP2007262084A (ja)	2007-10-11
FR2740132A1 (fr)	1997-04-25
BR9611223A (pt)	1999-04-06
NZ320161A (en)	1998-10-28
PT858440E (pt)	2002-07-31
KR19990066942A (ko)	1999-08-16
DK0858440T3 (da)	2002-04-29
EP0858440A1 (de)	1998-08-19
NO981800L (no)	1998-06-11
AU722645B2 (en)	2000-08-10
CZ291762B6 (cs)	2003-05-14
MX9803175A (es)	1998-09-30
SK282636B6 (sk)	2002-10-08
FR2740132B1 (fr)	1997-12-19
AR004079A1 (es)	1998-09-30
NO981800D0 (no)	1998-04-22
RO120193B1 (ro)	2005-10-28
NO309716B1 (no)	2001-03-19
IL124086A (en)	2000-06-29
EA001416B1 (ru)	2001-02-26
ATE211723T1 (de)	2002-01-15
ES2171228T3 (es)	2002-09-01
JP2000513705A (ja)	2000-10-17
US20040019244A1 (en)	2004-01-29
DE69618476D1 (de)	2002-02-14
JP2009084290A (ja)	2009-04-23
EA199800322A1 (ru)	1998-10-29
PL326367A1 (en)	1998-09-14
ZA968481B (en)	1997-05-20
DE69618476T2 (de)	2002-08-29
PL186534B1 (pl)	2004-01-30
CA2232421A1 (fr)	1997-05-01
CA2232421C (fr)	2008-12-02
US6930215B2 (en)	2005-08-16
EP0858440B1 (de)	2002-01-09
WO1997015540A1 (fr)	1997-05-01
HUP9802978A2 (hu)	1999-04-28
US20050256348A1 (en)	2005-11-17
CZ125498A3 (cs)	1998-07-15
HU222560B1 (hu)	2003-08-28
AU7284996A (en)	1997-05-15

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UA61895C2 (en)	2003-12-15	A method for preparing 1,1,1,3,3-pentafluoropropane
EP0876314B1 (de)	2003-02-26	Verfahren zur herstellung von halogenkohlenwasserstoffen und ausgewählte verbindungen und azeotrope mit hf
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KR100235757B1 (ko)	1999-12-15	퍼클로로에틸렌으로 부터 하이드로플루오로카본을 제조하는 일단계방법
AU8614998A (en)	1999-04-15	Synthesis of 1,1,1,3,3-pentafluoropropane
JP3130656B2 (ja)	2001-01-31	１，１−ジクロロ−１，３，３，３− テトラフルオロプロパンの製造法
JP2846713B2 (ja)	1999-01-13	高められた圧力の下に１，１，１‐トリフルオロ‐２，２‐ジクロロエタンを製造する方法
US7629496B2 (en)	2009-12-08	Process for the manufacture of 1,1,1,3,3-pentafluoropropane
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JPH08268931A (ja)	1996-10-15	ジフルオロメタンの製造方法