ZA200204981B - Fluorine containing allylethers and higher homologs. - Google Patents

Fluorine containing allylethers and higher homologs. Download PDF

Info

Publication number: ZA200204981B
Authority: ZA; South Africa
Prior art keywords: perfluorinated; ether; process according; compound; formula
Prior art date: 1999-12-22

Application number

ZA200204981A

Other languages

English (en)

Inventor

Jay F Schultz

Werner Schwertfeger

Zai-Ming Qui

Erik D Hare

George G I Moore

Klaus Hintzer

Miguel A Guerra

Allan T Worm

Original Assignee

Dyneon Llc

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.)

1999-12-22

Filing date

2002-06-20

Publication date

2003-11-27

2002-06-20 Application filed by Dyneon Llc filed Critical Dyneon Llc

2003-11-27 Publication of ZA200204981B publication Critical patent/ZA200204981B/en

Links

229910052731 fluorine Inorganic materials 0.000 title description 7
239000011737 fluorine Substances 0.000 title description 7
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title description 5
-1 1,2- dichloro propyl Chemical group 0.000 claims description 35
238000000034 method Methods 0.000 claims description 26
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims description 18
239000002243 precursor Substances 0.000 claims description 17
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
239000001257 hydrogen Substances 0.000 claims description 13
229910052739 hydrogen Inorganic materials 0.000 claims description 13
ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical class C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 claims description 11
150000002170 ethers Chemical class 0.000 claims description 11
238000002360 preparation method Methods 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 6
125000004430 oxygen atom Chemical group O* 0.000 claims description 6
125000001931 aliphatic group Chemical group 0.000 claims description 5
150000001336 alkenes Chemical class 0.000 claims description 5
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 5
239000003638 chemical reducing agent Substances 0.000 claims description 4
230000000382 dechlorinating effect Effects 0.000 claims description 3
238000006298 dechlorination reaction Methods 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims 1
239000000460 chlorine Substances 0.000 description 16
238000003682 fluorination reaction Methods 0.000 description 13
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
239000000047 product Substances 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000004821 distillation Methods 0.000 description 6
239000000203 mixture Substances 0.000 description 6
229910052801 chlorine Inorganic materials 0.000 description 5
PQMAKJUXOOVROI-UHFFFAOYSA-N 2,2,3,3,5,5,6,6-octafluoro-4-(trifluoromethyl)morpholine Chemical compound FC(F)(F)N1C(F)(F)C(F)(F)OC(F)(F)C1(F)F PQMAKJUXOOVROI-UHFFFAOYSA-N 0.000 description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
KLKFAASOGCDTDT-UHFFFAOYSA-N ethoxymethoxyethane Chemical compound CCOCOCC KLKFAASOGCDTDT-UHFFFAOYSA-N 0.000 description 4
HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 4
238000010992 reflux Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000007858 starting material Substances 0.000 description 4
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
239000002585 base Substances 0.000 description 3
125000001033 ether group Chemical group 0.000 description 3
229920001973 fluoroelastomer Polymers 0.000 description 3
239000011701 zinc Substances 0.000 description 3
ZXCYIJGIGSDJQQ-UHFFFAOYSA-N 2,3-dichloropropan-1-ol Chemical compound OCC(Cl)CCl ZXCYIJGIGSDJQQ-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
150000001348 alkyl chlorides Chemical group 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
229920002313 fluoropolymer Polymers 0.000 description 2
239000004811 fluoropolymer Substances 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
150000002739 metals Chemical class 0.000 description 2
230000005012 migration Effects 0.000 description 2
238000013508 migration Methods 0.000 description 2
239000000178 monomer Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
BLTXWCKMNMYXEA-UHFFFAOYSA-N 1,1,2-trifluoro-2-(trifluoromethoxy)ethene Chemical compound FC(F)=C(F)OC(F)(F)F BLTXWCKMNMYXEA-UHFFFAOYSA-N 0.000 description 1
BZPCMSSQHRAJCC-UHFFFAOYSA-N 1,2,3,3,4,4,5,5,5-nonafluoro-1-(1,2,3,3,4,4,5,5,5-nonafluoropent-1-enoxy)pent-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)=C(F)OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)F BZPCMSSQHRAJCC-UHFFFAOYSA-N 0.000 description 1
UKBFZYZBLPXEIL-UHFFFAOYSA-N 1,3-dichloro-1-(1,3-dichloro-1,2,2,3,3-pentafluoropropoxy)-1,2,2,3,3-pentafluoropropane Chemical compound FC(F)(Cl)C(F)(F)C(F)(Cl)OC(F)(Cl)C(F)(F)C(F)(F)Cl UKBFZYZBLPXEIL-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
IBTLFDCPAJLATQ-UHFFFAOYSA-N 1-prop-2-enoxybutane Chemical compound CCCCOCC=C IBTLFDCPAJLATQ-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
VNJOEUSYAMPBAK-UHFFFAOYSA-N 2-methylbenzenesulfonic acid;hydrate Chemical compound O.CC1=CC=CC=C1S(O)(=O)=O VNJOEUSYAMPBAK-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
229910003074 TiCl4 Inorganic materials 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 1
125000005336 allyloxy group Chemical group 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
ABDBNWQRPYOPDF-UHFFFAOYSA-N carbonofluoridic acid Chemical compound OC(F)=O ABDBNWQRPYOPDF-UHFFFAOYSA-N 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000001805 chlorine compounds Chemical group 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
150000003950 cyclic amides Chemical class 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000000806 elastomer Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
238000006053 organic reaction Methods 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
125000005459 perfluorocyclohexyl group Chemical group 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000000197 pyrolysis Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000008707 rearrangement Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/17—Unsaturated ethers containing halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/16—Preparation of ethers by reaction of esters of mineral or organic acids with hydroxy or O-metal groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/22—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of halogens; by substitution of halogen atoms by other halogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/24—Preparation of ethers by reactions not forming ether-oxygen bonds by elimination of halogens, e.g. elimination of HCl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/30—Compounds having groups
- C07C43/313—Compounds having groups containing halogen

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

ZA200204981A 1999-12-22 2002-06-20 Fluorine containing allylethers and higher homologs. ZA200204981B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US09/470,034 US6255535B1 (en)	1999-12-22	1999-12-22	Fluorine containing allylethers and higher homologs

Publications (1)

Publication Number	Publication Date
ZA200204981B true ZA200204981B (en)	2003-11-27

Family

ID=23866006

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200204981A ZA200204981B (en)	1999-12-22	2002-06-20	Fluorine containing allylethers and higher homologs.

Country Status (8)

Country	Link
US (1)	US6255535B1 (it)
EP (1)	EP1240126B1 (it)
JP (1)	JP2003518052A (it)
AU (1)	AU4712800A (it)
CA (1)	CA2393460A1 (it)
DE (1)	DE60026022T2 (it)
WO (1)	WO2001046108A1 (it)
ZA (1)	ZA200204981B (it)

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EP1208075B1 (en)	1999-08-31	2004-10-06	Asahi Glass Company Ltd.	Process for producing a vic-dichloro acid fluoride
US6794457B2 (en) *	2001-04-30	2004-09-21	3M Innovative Properties Company	Fluoropolymer curing system containing a nitrogen cure site monomer
US20050113609A1 (en) *	2002-07-03	2005-05-26	Asahi Glass Company Limited	Fluorine-containing unsaturated compound and method for its production
EP1535892A4 (en) *	2002-07-03	2006-08-02	Asahi Glass Co Ltd	UNSATURATED FLUORINE COMPOUND AND METHOD OF MANUFACTURING THE SAME
RU2006123335A (ru) *	2003-12-30	2008-02-10	ЗМ Инновейтив Пропертиз Компани (US)	Способ коагуляции фторполимеров и композиции
US7402630B2 (en) *	2004-12-16	2008-07-22	3M Innovative Properties Company	Curing compositions for fluoropolymers
GB0427913D0 (en) *	2004-12-21	2005-01-19	3M Innovative Properties Co	Fluoropolymer for making a fluoroelastomer
JP2006232704A (ja) *	2005-02-23	2006-09-07	Asahi Glass Co Ltd	新規なフルオロスルホニル基含有化合物
US7294677B2 (en) *	2005-08-25	2007-11-13	3M Innovative Properties Company	Catalyst for making fluoroelastomer compositions and methods of using the same
US7531701B2 (en) *	2006-09-12	2009-05-12	Honeywell International Inc.	Allyloxytrifluoropropenes
GB2459672A (en) *	2008-04-30	2009-11-04	3M Innovative Properties Co	Linear short-chained perfluorinated alkoxy allyl ethers and their preparation
WO2010151610A2 (en)	2009-06-25	2010-12-29	3M Innovative Properties Company	Curing compositions for fluoropolymers
EP2723711B1 (en) *	2011-06-27	2016-08-10	Solvay Specialty Polymers Italy S.p.A.	Novel fluorinated unsaturated compound and polymers obtainable therefrom
CN104093780B (zh)	2011-11-09	2016-09-14	3M创新有限公司	用于含氟聚合物的固化组合物
CN115960128A (zh) *	2014-12-19	2023-04-14	默克专利股份有限公司	氟化合物
WO2017083688A1 (en)	2015-11-13	2017-05-18	3M Innovative Properties Company	Compositions including a bimodal blend of amorphous fluoropolymers and their uses
EP3405504B1 (en)	2016-01-21	2021-07-21	3M Innovative Properties Company	Additive processing of fluoroelastomers
CN105503548A (zh) *	2016-01-26	2016-04-20	巨化集团技术中心	一种氟卤代烯醚的合成方法
TW201815845A (zh)	2016-05-17	2018-05-01	３Ｍ新設資產公司	包括二氟亞乙烯與四氟乙烯的共聚物之組成物及其使用方法
EP3559105B1 (en)	2016-12-20	2020-11-18	3M Innovative Properties Company	Filament based on a composition including fluoropolymer and inorganic filler and method of making a three-dimensional article
EP3896052A1 (en)	2017-05-19	2021-10-20	3M Innovative Properties Co.	Methods of making a polyfluorinated allyl ether and compounds relating to the methods
PL3728177T3 (pl)	2017-12-21	2022-05-30	3M Innovative Properties Company	Sposoby wytwarzania wielfunkcyjnych związków wielofluorowanych
CN113166499A (zh)	2018-09-24	2021-07-23	埃克森美孚化学专利公司	交联的弹性体-聚合物共混物
RU2018141773A (ru)	2018-11-27	2020-05-27	3М Инновейтив Пропертиз Компани	Композиции полимерных процессинговых добавок и изделия, полученные с использованием указанных композиций
TW202033573A (zh)	2018-12-17	2020-09-16	美商3M新設資產公司	包括可固化氟聚合物及固化劑之組成物及製造及使用其之方法
WO2020175674A1 (ja)	2019-02-28	2020-09-03	Ａｇｃ株式会社	スルホン酸基含有ポリマー、フルオロスルホニル基含有ポリマーおよび液状組成物
WO2020245724A1 (en)	2019-06-04	2020-12-10	3M Innovative Properties Company	Multifunctional fluorinated compound, fluorinated polymers made from the compound, and related methods
CN114302913A (zh)	2019-09-05	2022-04-08	3M创新有限公司	包含含氟聚合物和支链倍半硅氧烷聚合物的组合物和制品
WO2021137084A1 (en)	2019-12-30	2021-07-08	3M Innovative Properties Company	Composition including fluoropolymer, benzoyl peroxide, and crosslinker and related articles and methods
WO2021214664A1 (en)	2020-04-21	2021-10-28	3M Innovative Properties Company	Particles including polytetrafluoroethylene and process for making a three-dimensional article
US20240132643A1 (en)	2021-02-26	2024-04-25	3M Innovative Properties Company	Process for Making a Fluoropolymer and Fluoropolymer Made Therefrom
WO2022189938A1 (en)	2021-03-10	2022-09-15	3M Innovative Properties Company	Branched silsesquioxane polymer and compositions and articles including the same
WO2023224824A1 (en)	2022-05-17	2023-11-23	Dupont Specialty Products Usa, Llc	Method of making halo (alkyl vinyl) ether monomers and fluorinated polymers made with the halo (alkyl vinyl) ether monomer

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US4273728A (en)	1979-03-14	1981-06-16	E. I. Du Pont De Nemours And Company	Polyfluoroallyloxy compounds, their preparation and copolymers therefrom
JPS5759850A (en)	1980-09-30	1982-04-10	Daikin Ind Ltd	Polyfluoroallyl ether and its preparation and use
DE3045473A1 (de)	1980-12-03	1982-07-01	Hoechst Ag, 6000 Frankfurt	Verfahren zur herstellung von 2-alkenyl-1,1,2-trifluor-2-halogenethyl-ethern
US4522995A (en) *	1983-05-02	1985-06-11	E. I. Du Pont De Nemours And Company	Fluorinated alkyl ether-containing ethylenes, precursors thereto, and copolymers thereof with tetrafluoroethylene
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DE3718726A1 (de)	1987-06-04	1988-12-22	Hoechst Ag	Verfahren zur herstellung fluorierter vinylether
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US5488142A (en)	1993-10-04	1996-01-30	Minnesota Mining And Manufacturing Company	Fluorination in tubular reactor system
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US5891965A (en)	1997-01-06	1999-04-06	Dyneon Llc	Low temperature perfluoroether-containing fluoroelastomers
AU3204597A (en)	1997-05-02	1998-11-27	Minnesota Mining And Manufacturing Company	Electrochemical fluorination using interrupted current

1999
- 1999-12-22 US US09/470,034 patent/US6255535B1/en not_active Expired - Lifetime
2000
- 2000-05-12 JP JP2001546622A patent/JP2003518052A/ja active Pending
- 2000-05-12 EP EP00928975A patent/EP1240126B1/en not_active Expired - Lifetime
- 2000-05-12 CA CA002393460A patent/CA2393460A1/en not_active Abandoned
- 2000-05-12 DE DE60026022T patent/DE60026022T2/de not_active Expired - Lifetime
- 2000-05-12 WO PCT/US2000/013116 patent/WO2001046108A1/en active IP Right Grant
- 2000-05-12 AU AU47128/00A patent/AU4712800A/en not_active Abandoned
2002
- 2002-06-20 ZA ZA200204981A patent/ZA200204981B/en unknown

Also Published As

Publication number	Publication date
EP1240126B1 (en)	2006-02-15
DE60026022T2 (de)	2006-10-26
WO2001046108A1 (en)	2001-06-28
AU4712800A (en)	2001-07-03
JP2003518052A (ja)	2003-06-03
EP1240126A1 (en)	2002-09-18
DE60026022D1 (de)	2006-04-20
CA2393460A1 (en)	2001-05-28
US6255535B1 (en)	2001-07-03

Publication	Publication Date	Title
US6255535B1 (en)	2001-07-03	Fluorine containing allylethers and higher homologs
US6548719B1 (en)	2003-04-15	Process for producing fluoroolefins
EP1148041B1 (en)	2008-09-17	Fluorovinylethers and polymers obtainable therefrom
US7371904B2 (en)	2008-05-13	Processes for synthesis of 1,3,3,3-tetrafluoropropene
US7160967B2 (en)	2007-01-09	Fluorovinyl ethers and polymers obtainable therefrom
JP5101805B2 (ja)	2012-12-19	フルオロエラストマー
TWI432463B (zh)	2014-04-01	含氟彈性體
US7834097B2 (en)	2010-11-16	Fluoroelastomers
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