SK280442B6 - Spôsob hydroxykarbonylácie penténových kyselín - Google Patents

Spôsob hydroxykarbonylácie penténových kyselín Download PDF

Info

Publication number: SK280442B6
Authority: SK; Slovakia
Prior art keywords: reaction mixture; hydroxycarbonylation; catalyst; temperature; pentenoic
Prior art date: 1992-10-22

Application number

SK518-95A

Other languages

English (en)

Slovak (sk)

Other versions

SK51895A3 (en

Inventor

Philippe Denis

Francois Klinger

Jean-Claude Laurent

Robert Perron

Joel Schwartz

Francois Vachet

Original Assignee

Rhone-Poulenc Chimie

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.)

1992-10-22

Filing date

1993-10-19

Publication date

2000-02-14

1993-10-19 Application filed by Rhone-Poulenc Chimie filed Critical Rhone-Poulenc Chimie

1995-08-09 Publication of SK51895A3 publication Critical patent/SK51895A3/sk

2000-02-14 Publication of SK280442B6 publication Critical patent/SK280442B6/sk

Links

238000000034 method Methods 0.000 title claims abstract description 37
YIYBQIKDCADOSF-UHFFFAOYSA-N pentenoic acid group Chemical class C(C=CCC)(=O)O YIYBQIKDCADOSF-UHFFFAOYSA-N 0.000 title claims abstract description 33
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims abstract description 67
239000011541 reaction mixture Substances 0.000 claims abstract description 53
239000003054 catalyst Substances 0.000 claims abstract description 47
239000001361 adipic acid Substances 0.000 claims abstract description 33
235000011037 adipic acid Nutrition 0.000 claims abstract description 33
229910052741 iridium Inorganic materials 0.000 claims abstract description 27
GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims abstract description 27
YIYBQIKDCADOSF-ONEGZZNKSA-N trans-pent-2-enoic acid Chemical compound CC\C=C\C(O)=O YIYBQIKDCADOSF-ONEGZZNKSA-N 0.000 claims abstract description 19
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 18
229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 16
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract description 12
VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 claims abstract description 5
238000006243 chemical reaction Methods 0.000 claims description 32
238000007670 refining Methods 0.000 claims description 27
238000002425 crystallisation Methods 0.000 claims description 13
230000008025 crystallization Effects 0.000 claims description 13
239000000203 mixture Substances 0.000 claims description 13
238000000926 separation method Methods 0.000 claims description 13
239000002904 solvent Substances 0.000 claims description 10
239000013078 crystal Substances 0.000 claims description 9
125000001931 aliphatic group Chemical group 0.000 claims description 6
238000010438 heat treatment Methods 0.000 claims description 5
238000002844 melting Methods 0.000 claims description 5
230000008018 melting Effects 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
150000001875 compounds Chemical class 0.000 claims description 4
150000001735 carboxylic acids Chemical class 0.000 claims description 3
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
238000001816 cooling Methods 0.000 claims description 2
239000000374 eutectic mixture Substances 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
150000002430 hydrocarbons Chemical class 0.000 claims description 2
230000002000 scavenging effect Effects 0.000 claims description 2
239000002699 waste material Substances 0.000 claims 2
159000000032 aromatic acids Chemical class 0.000 claims 1
125000003118 aryl group Chemical group 0.000 claims 1
239000012141 concentrate Substances 0.000 claims 1
150000002170 ethers Chemical class 0.000 claims 1
229910052703 rhodium Inorganic materials 0.000 abstract description 2
239000010948 rhodium Substances 0.000 abstract description 2
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 abstract description 2
229960000250 adipic acid Drugs 0.000 description 29
GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 14
239000012071 phase Substances 0.000 description 14
UIUWNILCHFBLEQ-NSCUHMNNSA-N trans-pent-3-enoic acid Chemical compound C\C=C\CC(O)=O UIUWNILCHFBLEQ-NSCUHMNNSA-N 0.000 description 12
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 11
229910052740 iodine Inorganic materials 0.000 description 11
239000011630 iodine Substances 0.000 description 11
239000007788 liquid Substances 0.000 description 11
RVHOBHMAPRVOLO-UHFFFAOYSA-N 2-ethylbutanedioic acid Chemical compound CCC(C(O)=O)CC(O)=O RVHOBHMAPRVOLO-UHFFFAOYSA-N 0.000 description 8
229910052751 metal Inorganic materials 0.000 description 8
239000002184 metal Substances 0.000 description 8
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 8
XJMMNTGIMDZPMU-UHFFFAOYSA-N 3-methylglutaric acid Chemical compound OC(=O)CC(C)CC(O)=O XJMMNTGIMDZPMU-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
150000001991 dicarboxylic acids Chemical class 0.000 description 6
HVAMZGADVCBITI-UHFFFAOYSA-N pent-4-enoic acid Chemical compound OC(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-N 0.000 description 6
229910052705 radium Inorganic materials 0.000 description 6
HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 6
WVUYYXUATWMVIT-UHFFFAOYSA-N 1-bromo-4-ethoxybenzene Chemical compound CCOC1=CC=C(Br)C=C1 WVUYYXUATWMVIT-UHFFFAOYSA-N 0.000 description 5
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 5
229910000043 hydrogen iodide Inorganic materials 0.000 description 5
239000002253 acid Substances 0.000 description 4
238000004821 distillation Methods 0.000 description 4
238000004064 recycling Methods 0.000 description 4
229940005605 valeric acid Drugs 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 3
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
239000013529 heat transfer fluid Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
-1 aromatic carboxylic acids Chemical class 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
238000000605 extraction Methods 0.000 description 2
238000004817 gas chromatography Methods 0.000 description 2
238000004128 high performance liquid chromatography Methods 0.000 description 2
238000009776 industrial production Methods 0.000 description 2
239000007791 liquid phase Substances 0.000 description 2
MKUWVMRNQOOSAT-UHFFFAOYSA-N methylvinylmethanol Natural products CC(O)C=C MKUWVMRNQOOSAT-UHFFFAOYSA-N 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
239000004912 1,5-cyclooctadiene Substances 0.000 description 1
WCASXYBKJHWFMY-NSCUHMNNSA-N 2-Buten-1-ol Chemical class C\C=C\CO WCASXYBKJHWFMY-NSCUHMNNSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
YAMMTDRSRBOHDL-UHFFFAOYSA-N [Ir].[I] Chemical compound [Ir].[I] YAMMTDRSRBOHDL-UHFFFAOYSA-N 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
150000001351 alkyl iodides Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
229960004365 benzoic acid Drugs 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000010408 film Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000002779 inactivation Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
235000014666 liquid concentrate Nutrition 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000005527 organic iodine compounds Chemical class 0.000 description 1
239000003279 phenylacetic acid Substances 0.000 description 1
229960003424 phenylacetic acid Drugs 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
238000011084 recovery Methods 0.000 description 1
230000008929 regeneration Effects 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
239000000523 sample Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000003068 static effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000010409 thin film Substances 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-M valerate Chemical class CCCCC([O-])=O NQPDZGIKBAWPEJ-UHFFFAOYSA-M 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000004876 x-ray fluorescence Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C55/00—Saturated compounds having more than one carboxyl group bound to acyclic carbon atoms
- C07C55/02—Dicarboxylic acids
- C07C55/14—Adipic acid
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/14—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
- 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
- Y02P20/584—Recycling of catalysts

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Crystallography & Structural Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

SK518-95A 1992-10-22 1993-10-19 Spôsob hydroxykarbonylácie penténových kyselín SK280442B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR9212913A FR2697247B1 (fr)	1992-10-22	1992-10-22	Procédé d'hydroxycarbonylation d'acides penténoiques.
PCT/FR1993/001028 WO1994008939A1 (fr)	1992-10-22	1993-10-19	Procede d'hydroxycarbonylation d'acides pentenoiques

Publications (2)

Publication Number	Publication Date
SK51895A3 SK51895A3 (en)	1995-08-09
SK280442B6 true SK280442B6 (sk)	2000-02-14

Family

ID=9434963

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK518-95A SK280442B6 (sk)	1992-10-22	1993-10-19	Spôsob hydroxykarbonylácie penténových kyselín

Country Status (18)

Country	Link
US (1)	US6008408A (de)
EP (1)	EP0665828B1 (de)
JP (1)	JP2895233B2 (de)
KR (1)	KR0185232B1 (de)
CN (1)	CN1034660C (de)
BR (1)	BR9307284A (de)
CA (1)	CA2146975A1 (de)
CZ (1)	CZ286694B6 (de)
DE (1)	DE69310193T2 (de)
ES (1)	ES2100575T3 (de)
FR (1)	FR2697247B1 (de)
PL (1)	PL175043B1 (de)
RU (1)	RU2119477C1 (de)
SG (1)	SG70989A1 (de)
SK (1)	SK280442B6 (de)
TW (1)	TW252102B (de)
UA (1)	UA44228C2 (de)
WO (1)	WO1994008939A1 (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5292944A (en) *	1993-06-29	1994-03-08	E. I. Du Pont De Nemours And Company	Process for the preparation of adipic acid or pentenoic acid
FR2749299B1 (fr) *	1996-06-04	1998-07-17	Rhone Poulenc Fibres	Procede de purification de l'acide adipique dans l'eau
TW200633970A (en) *	2005-02-11	2006-10-01	Shell Int Research	Process for the preparation of a dicarboxylic acid
CN101142161A (zh) *	2005-02-11	2008-03-12	国际壳牌研究有限公司	共轭二烯的羰基化方法
CN101137610A (zh) *	2005-02-11	2008-03-05	国际壳牌研究有限公司	二羧酸的制备方法
CN101137612A (zh) *	2005-02-11	2008-03-05	国际壳牌研究有限公司	二羧酸的制备方法
US20080269520A1 (en) *	2005-02-11	2008-10-30	Eit Drent	Process for the Carbonylation of a Conjugated Diene to a Dicarboxylic Acid
WO2006125801A1 (en) *	2005-05-27	2006-11-30	Shell Internationale Research Maatschappij B.V.	Process for the preparation of adipic acid from n-pentenoic acid
CN115445662B (zh) *	2022-08-31	2023-08-15	迈奇化学股份有限公司	γ-丁内酯羰基化用催化剂及由γ-丁内酯合成戊二酸的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA512911A (en) *		1955-05-17	B. Clark William	Adipic acid crystallization
US2910516A (en) *	1953-08-20	1959-10-27	Phillips Petroleum Co	Fractional crystallization process and apparatus
NL255708A (de) *	1959-09-08
US4788333A (en) *	1985-01-07	1988-11-29	E. I. Du Pont De Nemours And Company	Hydrocarboxylation of unsaturated carboxylic acids to linear dicarboxylic acids
FR2666808B1 (fr) *	1990-09-18	1994-04-01	Rhone Poulenc Chimie	Procede de preparation de l'acide adipique par hydrocarboxylation d'acides penteniques.
US5166421A (en) *	1991-03-18	1992-11-24	E. I. Du Pont De Nemours And Company	Process for the manufacture of adipic acid

1992
- 1992-10-22 FR FR9212913A patent/FR2697247B1/fr not_active Expired - Fee Related
1993
- 1993-10-04 TW TW082108170A patent/TW252102B/zh active
- 1993-10-19 KR KR1019950701488A patent/KR0185232B1/ko not_active IP Right Cessation
- 1993-10-19 ES ES93924095T patent/ES2100575T3/es not_active Expired - Lifetime
- 1993-10-19 RU RU95109575A patent/RU2119477C1/ru not_active IP Right Cessation
- 1993-10-19 DE DE69310193T patent/DE69310193T2/de not_active Expired - Fee Related
- 1993-10-19 SG SG1996008354A patent/SG70989A1/en unknown
- 1993-10-19 BR BR9307284A patent/BR9307284A/pt not_active IP Right Cessation
- 1993-10-19 CZ CZ19951013A patent/CZ286694B6/cs not_active IP Right Cessation
- 1993-10-19 CA CA002146975A patent/CA2146975A1/fr not_active Abandoned
- 1993-10-19 EP EP93924095A patent/EP0665828B1/de not_active Expired - Lifetime
- 1993-10-19 PL PL93308300A patent/PL175043B1/pl not_active IP Right Cessation
- 1993-10-19 WO PCT/FR1993/001028 patent/WO1994008939A1/fr active IP Right Grant
- 1993-10-19 US US08/424,335 patent/US6008408A/en not_active Expired - Fee Related
- 1993-10-19 SK SK518-95A patent/SK280442B6/sk unknown
- 1993-10-19 UA UA95038271A patent/UA44228C2/uk unknown
- 1993-10-19 JP JP6509714A patent/JP2895233B2/ja not_active Expired - Lifetime
- 1993-10-21 CN CN93119171A patent/CN1034660C/zh not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JPH08501726A (ja)	1996-02-27
CN1034660C (zh)	1997-04-23
FR2697247A1 (fr)	1994-04-29
DE69310193D1 (de)	1997-05-28
EP0665828B1 (de)	1997-04-23
BR9307284A (pt)	1999-05-11
CA2146975A1 (fr)	1994-04-28
KR950703507A (ko)	1995-09-20
WO1994008939A1 (fr)	1994-04-28
JP2895233B2 (ja)	1999-05-24
ES2100575T3 (es)	1997-06-16
RU95109575A (ru)	1996-12-27
DE69310193T2 (de)	1997-10-30
PL308300A1 (en)	1995-07-24
CN1090840A (zh)	1994-08-17
KR0185232B1 (ko)	1999-05-15
UA44228C2 (uk)	2002-02-15
PL175043B1 (pl)	1998-10-30
TW252102B (de)	1995-07-21
EP0665828A1 (de)	1995-08-09
US6008408A (en)	1999-12-28
CZ286694B6 (en)	2000-06-14
RU2119477C1 (ru)	1998-09-27
CZ101395A3 (en)	1995-10-18
FR2697247B1 (fr)	1994-12-02
SK51895A3 (en)	1995-08-09
SG70989A1 (en)	2000-03-21

Publication	Publication Date	Title
SK280442B6 (sk)	2000-02-14	Spôsob hydroxykarbonylácie penténových kyselín
US4246195A (en)	1981-01-20	Purification of carbonylation products
DE60006219T2 (de)	2004-04-22	Kontinuierliches verfahren zur herstellung von diacetoxybuten
US5227522A (en)	1993-07-13	Preparation of adipic acid by hydrocarboxylation of pentenic acids
AU641056B2 (en)	1993-09-09	Continuous process for the simultaneous preparation of acetic acid and acetic anhydride
WO1992016476A2 (en)	1992-10-01	Process for the manufacture of adipic acid
KR910009350B1 (ko)	1991-11-12	N-포르밀 아스파르트산 무수물의 제조방법
JP2808267B2 (ja)	1998-10-08	ブタジエンのヒドロキシカルボニル化方法
EP0578591B1 (de)	1997-10-15	Verfahren zur Herstellung von Adipinsäure durch Hydrocarboxylierung der Pentensäuren
JPH08225485A (ja)	1996-09-03	アジピン酸を得るための方法
KR100332256B1 (ko)	2002-07-18	펜테노산의히드록시카르보닐화방법
KR100250337B1 (ko)	2000-04-01	펜텐산의 히드로카르복실화에 의한 아디프산의 제조방법
US6967257B1 (en)	2005-11-22	Method of purifying lactic acid esters
CA2058043C (fr)	1996-07-23	Procede de preparation de l'acide adipique par hydroxycarboxylation d'acides penteniques
JP3682805B2 (ja)	2005-08-17	飽和脂肪族カルボン酸アミドの製造方法
JPS59110645A (ja)	1984-06-26	純粋なクロトン酸の製造方法
JP3565586B2 (ja)	2004-09-15	脂肪酸エステルの精製方法
FR2703045A1 (fr)	1994-09-30	Procédé d'isomérisation d'acides carboxyliques.
JPS6146468B2 (de)	1986-10-14
JP2003342227A (ja)	2003-12-03	ビフェニルテトラカルボン酸の製造法
JPH10218832A (ja)	1998-08-18	アクリル酸の精製法
CZ287699B6 (en)	2001-01-17	Carbonylation process of allylic butenols and esters thereof
MXPA98010305A (es)	2000-01-01	Procedimiento de hidroxicarbonilacion de los acidos pentenoicos
JPS6044398B2 (ja)	1985-10-03	高級二塩基酸ジメチルの製造方法
WO2001081300A1 (fr)	2001-11-01	Procede de cristallisation d'acide 2-acetylthio-3-phenylpropionique