CA2491207C - Procede de synthese de derives a radical hydrogenofluoromethylenesulfonyle - Google Patents
Procede de synthese de derives a radical hydrogenofluoromethylenesulfonyle Download PDFInfo
- Publication number
- CA2491207C CA2491207C CA2491207A CA2491207A CA2491207C CA 2491207 C CA2491207 C CA 2491207C CA 2491207 A CA2491207 A CA 2491207A CA 2491207 A CA2491207 A CA 2491207A CA 2491207 C CA2491207 C CA 2491207C
- Authority
- CA
- Canada
- Prior art keywords
- equal
- water
- fluorine
- solvent
- fact
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title claims abstract description 22
- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 17
- 238000003786 synthesis reaction Methods 0.000 title claims abstract description 13
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 24
- 239000011737 fluorine Substances 0.000 claims abstract description 24
- -1 sulphide salt Chemical class 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 18
- 150000007944 thiolates Chemical class 0.000 claims abstract description 14
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 12
- 239000000460 chlorine Substances 0.000 claims abstract description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 10
- 150000002367 halogens Chemical class 0.000 claims abstract description 10
- 239000001257 hydrogen Substances 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 36
- 239000002904 solvent Substances 0.000 claims description 29
- 239000002253 acid Substances 0.000 claims description 20
- 239000008346 aqueous phase Substances 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 19
- 150000004820 halides Chemical class 0.000 claims description 18
- 150000001768 cations Chemical class 0.000 claims description 17
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 9
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 5
- 238000009396 hybridization Methods 0.000 claims description 5
- 239000003125 aqueous solvent Substances 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 230000002051 biphasic effect Effects 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 125000005496 phosphonium group Chemical group 0.000 claims description 2
- 239000002798 polar solvent Substances 0.000 claims description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 239000011630 iodine Substances 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 15
- 239000012071 phase Substances 0.000 description 11
- 239000002585 base Substances 0.000 description 9
- 229910052717 sulfur Inorganic materials 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- UENWRTRMUIOCKN-UHFFFAOYSA-N benzyl thiol Chemical compound SCC1=CC=CC=C1 UENWRTRMUIOCKN-UHFFFAOYSA-N 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000005660 chlorination reaction Methods 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 238000005658 halogenation reaction Methods 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 3
- 150000003568 thioethers Chemical group 0.000 description 3
- 230000009466 transformation Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 125000001743 benzylic group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- JYQLKKNUGGVARY-UHFFFAOYSA-N difluoromethanesulfonyl chloride Chemical compound FC(F)S(Cl)(=O)=O JYQLKKNUGGVARY-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 230000026030 halogenation Effects 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 2
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
- 150000003461 sulfonyl halides Chemical class 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical class ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- UFHFLCQGNIYNRP-VVKOMZTBSA-N Dideuterium Chemical compound [2H][2H] UFHFLCQGNIYNRP-VVKOMZTBSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 101100369068 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) TDA1 gene Proteins 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- PFTYKBCYTNZWCX-UHFFFAOYSA-N difluoromethanesulfinic acid Chemical compound OS(=O)C(F)F PFTYKBCYTNZWCX-UHFFFAOYSA-N 0.000 description 1
- CGDXUTMWWHKMOE-UHFFFAOYSA-N difluoromethanesulfonic acid Chemical compound OS(=O)(=O)C(F)F CGDXUTMWWHKMOE-UHFFFAOYSA-N 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- DHORGPSUEOTGTL-UHFFFAOYSA-N difluoromethylsulfanyl(difluoro)methane Chemical compound FC(F)SC(F)F DHORGPSUEOTGTL-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000000622 liquid--liquid extraction Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229940126601 medicinal product Drugs 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- YQCIWBXEVYWRCW-UHFFFAOYSA-N methane;sulfane Chemical compound C.S YQCIWBXEVYWRCW-UHFFFAOYSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000008379 phenol ethers Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/02—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
- C07C303/16—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by oxidation of thiols, sulfides, hydropolysulfides, or polysulfides with formation of sulfo or halosulfonyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogen, Water And Hydrids (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR02/08090 | 2002-06-28 | ||
| FR0208090A FR2841551B1 (fr) | 2002-06-28 | 2002-06-28 | Procede de synthese de derives a radical hydrogenofluoromethylene-sulfonyle |
| PCT/FR2003/001940 WO2004002951A2 (fr) | 2002-06-28 | 2003-06-24 | Procede de synthese de derives a radical hydrogenofluoromethylenesulfonyle |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2491207A1 CA2491207A1 (fr) | 2004-01-08 |
| CA2491207C true CA2491207C (fr) | 2012-02-21 |
Family
ID=29724975
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2491207A Expired - Fee Related CA2491207C (fr) | 2002-06-28 | 2003-06-24 | Procede de synthese de derives a radical hydrogenofluoromethylenesulfonyle |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7534906B2 (https=) |
| EP (1) | EP1517888B1 (https=) |
| JP (1) | JP4531561B2 (https=) |
| CN (1) | CN100509776C (https=) |
| AT (1) | ATE395331T1 (https=) |
| AU (1) | AU2003260623A1 (https=) |
| CA (1) | CA2491207C (https=) |
| DE (1) | DE60320994D1 (https=) |
| FR (1) | FR2841551B1 (https=) |
| RU (1) | RU2346934C2 (https=) |
| WO (1) | WO2004002951A2 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101110602B (zh) * | 2006-07-20 | 2010-05-12 | 上海高清数字科技产业有限公司 | 基于多状态控制的载波捕获系统和方法 |
| RU2495878C2 (ru) | 2007-12-21 | 2013-10-20 | Ф.Хоффманн-Ля Рош Аг | Гетероциклические антивирусные соединения |
| RU2409559C1 (ru) * | 2009-08-03 | 2011-01-20 | Павел Анатольевич Семенов | Способ получения 1,1-дифторэтансульфохлорида |
| CN110028390B (zh) * | 2019-05-28 | 2022-01-14 | 深圳大学 | 烷基二氟甲基醚类化合物的合成方法 |
| CN115594617B (zh) * | 2022-07-29 | 2024-02-06 | 苏州翔实医药发展有限公司 | 一种二氟甲基磺酰氯的合成方法 |
| CN116063208A (zh) * | 2023-02-13 | 2023-05-05 | 安徽省化工研究院 | 一种二氟甲烷磺酰氯的合成方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2469401A1 (fr) * | 1979-11-13 | 1981-05-22 | Rhone Poulenc Ind | Procede de preparation de difluoromethane sulfonates alcalins |
| JPS5780366A (en) * | 1980-11-06 | 1982-05-19 | Sagami Chem Res Center | Bromodifluoromethyl sulfide and its preparation |
| JPS57146749A (en) * | 1981-01-29 | 1982-09-10 | Ici Ltd | Difluoromethane sulfonic acid and manufacture |
| FR2540108B1 (fr) * | 1983-02-02 | 1985-12-27 | Rhone Poulenc Spec Chim | Procede de preparation de perhalogenoalkylthioethers |
| FR2599366B1 (fr) * | 1986-05-28 | 1988-08-26 | Rhone Poulenc Spec Chim | Procede de preparation du sulfure de benzyle et de trifluoromethyle |
| EP0313939B1 (en) * | 1987-10-26 | 1992-09-16 | ATOCHEM NORTH AMERICA, INC. (a Pennsylvania corp.) | Oxidation of thiols, disulfides and thiolsulfonates |
| DE3741309A1 (de) * | 1987-12-05 | 1989-06-15 | Bayer Ag | Verfahren zur herstellung von trifluormethansulfonsaeurechlorid |
| DE4333058A1 (de) * | 1993-09-29 | 1995-03-30 | Hoechst Ag | Verfahren zur Herstellung von Trifluorethylschwefelverbindungen aus Thiolaten und 1-Chlor-2,2,2-trifluorethan |
| JP3638357B2 (ja) * | 1994-11-01 | 2005-04-13 | 東洋化成工業株式会社 | ２，２−ジアルキル−３−アセトキシプロパンスルフォニルクロリドを製造する方法 |
| FR2730993B1 (fr) * | 1995-02-28 | 1997-04-04 | Rhone Poulenc Chimie | Procede de synthese de compose hydrocarbone fluore sur un carbone d'une chaine alcoyle |
| IL117534A0 (en) * | 1995-03-24 | 1996-07-23 | Rhone Poulenc Agrochimie | Reagent and process which are useful for grafting a substituted difluoromethyl group onto a compound containing at least one electrophilic function |
| FR2743072B1 (fr) * | 1995-12-27 | 1998-02-27 | Electricite De France | Procede de preparation d'acides perfluoroalcanecarboxyliques et perfluoroalcanesulfoniques |
-
2002
- 2002-06-28 FR FR0208090A patent/FR2841551B1/fr not_active Expired - Fee Related
-
2003
- 2003-06-24 RU RU2005102101/04A patent/RU2346934C2/ru not_active IP Right Cessation
- 2003-06-24 AT AT03761633T patent/ATE395331T1/de not_active IP Right Cessation
- 2003-06-24 CN CNB038179326A patent/CN100509776C/zh not_active Expired - Lifetime
- 2003-06-24 AU AU2003260623A patent/AU2003260623A1/en not_active Abandoned
- 2003-06-24 JP JP2004516858A patent/JP4531561B2/ja not_active Expired - Lifetime
- 2003-06-24 DE DE60320994T patent/DE60320994D1/de not_active Expired - Lifetime
- 2003-06-24 WO PCT/FR2003/001940 patent/WO2004002951A2/fr not_active Ceased
- 2003-06-24 EP EP03761633A patent/EP1517888B1/fr not_active Expired - Lifetime
- 2003-06-24 US US10/519,287 patent/US7534906B2/en not_active Expired - Fee Related
- 2003-06-24 CA CA2491207A patent/CA2491207C/fr not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004002951A3 (fr) | 2004-04-15 |
| US7534906B2 (en) | 2009-05-19 |
| WO2004002951A2 (fr) | 2004-01-08 |
| EP1517888B1 (fr) | 2008-05-14 |
| CA2491207A1 (fr) | 2004-01-08 |
| FR2841551B1 (fr) | 2006-01-13 |
| JP4531561B2 (ja) | 2010-08-25 |
| US20060178536A1 (en) | 2006-08-10 |
| RU2346934C2 (ru) | 2009-02-20 |
| CN1671657A (zh) | 2005-09-21 |
| FR2841551A1 (fr) | 2004-01-02 |
| JP2005531626A (ja) | 2005-10-20 |
| CN100509776C (zh) | 2009-07-08 |
| EP1517888A2 (fr) | 2005-03-30 |
| RU2005102101A (ru) | 2005-08-27 |
| AU2003260623A1 (en) | 2004-01-19 |
| DE60320994D1 (de) | 2008-06-26 |
| ATE395331T1 (de) | 2008-05-15 |
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