RU2252210C2 - Способ получения vic-дихлорфторангидрида - Google Patents
Способ получения vic-дихлорфторангидрида Download PDFInfo
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- RU2252210C2 RU2252210C2 RU2002107994/04A RU2002107994A RU2252210C2 RU 2252210 C2 RU2252210 C2 RU 2252210C2 RU 2002107994/04 A RU2002107994/04 A RU 2002107994/04A RU 2002107994 A RU2002107994 A RU 2002107994A RU 2252210 C2 RU2252210 C2 RU 2252210C2
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- compound
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- fluorinated
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- ococf
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- 239000011701 zinc Substances 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- LFMIQNJMJJKICW-UHFFFAOYSA-N 1,1,2-trichloro-2-fluoroethene Chemical group FC(Cl)=C(Cl)Cl LFMIQNJMJJKICW-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- SXAMGRAIZSSWIH-UHFFFAOYSA-N 2-[3-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,2,4-oxadiazol-5-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NOC(=N1)CC(=O)N1CC2=C(CC1)NN=N2 SXAMGRAIZSSWIH-UHFFFAOYSA-N 0.000 description 1
- IHCCLXNEEPMSIO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 IHCCLXNEEPMSIO-UHFFFAOYSA-N 0.000 description 1
- COAUHYBSXMIJDK-UHFFFAOYSA-N 3,3-dichloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)C(Cl)Cl COAUHYBSXMIJDK-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920001774 Perfluoroether Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical group [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000010504 bond cleavage reaction Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000006298 dechlorination reaction Methods 0.000 description 1
- UXGNZZKBCMGWAZ-UHFFFAOYSA-N dimethylformamide dmf Chemical compound CN(C)C=O.CN(C)C=O UXGNZZKBCMGWAZ-UHFFFAOYSA-N 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000004334 fluoridation Methods 0.000 description 1
- CJXGPJZUDUOZDX-UHFFFAOYSA-N fluoromethanone Chemical group F[C]=O CJXGPJZUDUOZDX-UHFFFAOYSA-N 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- UJMWVICAENGCRF-UHFFFAOYSA-N oxygen difluoride Chemical class FOF UJMWVICAENGCRF-UHFFFAOYSA-N 0.000 description 1
- 229950011087 perflunafene Drugs 0.000 description 1
- UWEYRJFJVCLAGH-IJWZVTFUSA-N perfluorodecalin Chemical compound FC1(F)C(F)(F)C(F)(F)C(F)(F)[C@@]2(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)[C@@]21F UWEYRJFJVCLAGH-IJWZVTFUSA-N 0.000 description 1
- 239000010702 perfluoropolyether Substances 0.000 description 1
- RVZRBWKZFJCCIB-UHFFFAOYSA-N perfluorotributylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RVZRBWKZFJCCIB-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical group FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/708—Ethers
-
- 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
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/125—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups
- C07C59/135—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
- C07C67/287—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/63—Halogen-containing esters of saturated acids
-
- 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)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11/246154 | 1999-08-31 | ||
| JP24615499 | 1999-08-31 | ||
| JP2000/211722 | 2000-07-12 | ||
| JP2000211722 | 2000-07-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2002107994A RU2002107994A (ru) | 2003-11-27 |
| RU2252210C2 true RU2252210C2 (ru) | 2005-05-20 |
Family
ID=26537593
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2002107994/04A RU2252210C2 (ru) | 1999-08-31 | 2000-08-30 | Способ получения vic-дихлорфторангидрида |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6833477B2 (enExample) |
| EP (1) | EP1208075B1 (enExample) |
| JP (1) | JP4626118B2 (enExample) |
| KR (1) | KR100704527B1 (enExample) |
| CN (1) | CN1167662C (enExample) |
| AT (1) | ATE278657T1 (enExample) |
| AU (1) | AU6866000A (enExample) |
| CA (1) | CA2381351C (enExample) |
| DE (1) | DE60014673T2 (enExample) |
| RU (1) | RU2252210C2 (enExample) |
| WO (1) | WO2001016085A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1164122B1 (en) | 1999-03-23 | 2007-07-18 | Asahi Glass Company Ltd. | Process for producing fluorine compound through liquid-phase fluorination |
| JP4956856B2 (ja) * | 1999-12-20 | 2012-06-20 | 旭硝子株式会社 | フルオリド化合物の製造方法 |
| WO2001046093A2 (en) * | 1999-12-20 | 2001-06-28 | Asahi Glass Company, Limited | Process for producing a fluoride compound |
| AU2001236108A1 (en) * | 2000-06-02 | 2001-12-17 | Asahi Glass Company, Limited | Process for preparing unsaturated compounds by pyrolysis |
| CA2415620C (en) | 2000-07-11 | 2009-09-08 | Asahi Glass Company, Limited | Method for producing fluorine-containing compound |
| AU2001292268A1 (en) | 2000-09-27 | 2002-04-08 | Asahi Glass Company, Limited | Process for producing fluorinated ester compound |
| JPWO2002026689A1 (ja) * | 2000-09-27 | 2004-02-05 | 旭硝子株式会社 | 含フッ素多価カルボニル化合物の製造方法 |
| DE60224554T2 (de) * | 2001-10-30 | 2009-01-08 | Asahi Glass Co., Ltd. | Fluorsulfonylverbindungen und verfahren zur herstellung von davon abgeleiteten verbindungen |
| US7247757B2 (en) | 2004-10-06 | 2007-07-24 | Fujifilm Corporation | Method of producing a fluorine-containing vinyl ether compound |
| CN100338012C (zh) * | 2005-11-07 | 2007-09-19 | 上海泰卓科技有限公司 | 一种含氟酰氟类化合物的处理方法 |
| JP5416587B2 (ja) | 2006-10-03 | 2014-02-12 | メキシケム、アマンコ、ホールディング、ソシエダッド、アノニマ、デ、カピタル、バリアブレ | プロセス |
| JP2009203172A (ja) * | 2008-02-26 | 2009-09-10 | Fujifilm Corp | パーフルオロ多官能ビニルエーテル化合物の製造方法 |
| CN114085142B (zh) * | 2021-10-28 | 2024-08-20 | 浙江诺亚氟化工有限公司 | 一种含氟醚类化合物气相氧化裂解反应合成酰氟类化合物的方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2043328C1 (ru) * | 1993-01-11 | 1995-09-10 | Российский научный центр "Прикладная химия" | Способ получения мономеров |
| US5466877A (en) * | 1994-03-15 | 1995-11-14 | Minnesota Mining And Manufacturing Company | Process for converting perfluorinated esters to perfluorinated acyl fluorides and/or ketones |
| US5674949A (en) * | 1988-09-28 | 1997-10-07 | Exfluor Research Corporation | Liquid-phase fluorination |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3900372A (en) | 1974-09-16 | 1975-08-19 | Phillips Petroleum Co | Recycle of acyl fluoride and electrochemical fluorination of esters |
| JPS54135722A (en) * | 1978-04-12 | 1979-10-22 | Toyo Soda Mfg Co Ltd | Preparation of fluorine-containing ether |
| US4420638A (en) * | 1982-03-02 | 1983-12-13 | E. I. Du Pont De Nemours And Company | Fluorinated ether-ketones |
| US5322904A (en) | 1988-09-28 | 1994-06-21 | Exfluor Research Corporation | Liquid-phase fluorination |
| US5332790A (en) | 1988-09-28 | 1994-07-26 | Exfluor Research Corporation | Liquid-phase fluorination |
| JP2701454B2 (ja) * | 1989-05-24 | 1998-01-21 | 旭硝子株式会社 | 新規含フッ素化合物，その製造方法及び用途 |
| US5658785A (en) * | 1994-06-06 | 1997-08-19 | Children's Hospital, Inc. | Adeno-associated virus materials and methods |
| EP0822941B1 (en) * | 1995-04-19 | 2002-06-12 | Polymun Scientific Immunbiologische Forschung GmbH | Monoclonal antibodies against hiv-1 and vaccines made thereof |
| US6002055A (en) * | 1996-02-23 | 1999-12-14 | E. I. Du Pont De Nemours And Company | Process for making dihalodifluoromethanes and their homologues |
| US5846946A (en) * | 1996-06-14 | 1998-12-08 | Pasteur Merieux Serums Et Vaccins | Compositions and methods for administering Borrelia DNA |
| US6077662A (en) * | 1996-11-27 | 2000-06-20 | Emory University | Virus-like particles, methods and immunogenic compositions |
| US6054312A (en) * | 1997-08-29 | 2000-04-25 | Selective Genetics, Inc. | Receptor-mediated gene delivery using bacteriophage vectors |
| US6156952A (en) * | 1998-04-09 | 2000-12-05 | Constituent Institution Of The University Of Maryland System | HIV transgenic animals and uses therefor |
| AUPP349698A0 (en) * | 1998-05-13 | 1998-06-04 | Altronic Distributors Pty Ltd | Mounting assembly |
| JP2000154158A (ja) * | 1998-11-18 | 2000-06-06 | Asahi Glass Co Ltd | 含フッ素化合物およびその製法 |
| JP2001139509A (ja) * | 1999-08-31 | 2001-05-22 | Asahi Glass Co Ltd | 熱分解反応による不飽和化合物の製造方法 |
| US6255535B1 (en) | 1999-12-22 | 2001-07-03 | Dyneon Llc | Fluorine containing allylethers and higher homologs |
-
2000
- 2000-08-30 WO PCT/JP2000/005888 patent/WO2001016085A1/en not_active Ceased
- 2000-08-30 KR KR1020027002651A patent/KR100704527B1/ko not_active Expired - Lifetime
- 2000-08-30 EP EP00956818A patent/EP1208075B1/en not_active Expired - Lifetime
- 2000-08-30 RU RU2002107994/04A patent/RU2252210C2/ru active
- 2000-08-30 AT AT00956818T patent/ATE278657T1/de not_active IP Right Cessation
- 2000-08-30 DE DE60014673T patent/DE60014673T2/de not_active Expired - Lifetime
- 2000-08-30 CA CA002381351A patent/CA2381351C/en not_active Expired - Fee Related
- 2000-08-30 CN CNB008119902A patent/CN1167662C/zh not_active Expired - Lifetime
- 2000-08-30 JP JP2001519655A patent/JP4626118B2/ja not_active Expired - Lifetime
- 2000-08-30 AU AU68660/00A patent/AU6866000A/en not_active Abandoned
-
2002
- 2002-02-28 US US10/084,506 patent/US6833477B2/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5674949A (en) * | 1988-09-28 | 1997-10-07 | Exfluor Research Corporation | Liquid-phase fluorination |
| RU2043328C1 (ru) * | 1993-01-11 | 1995-09-10 | Российский научный центр "Прикладная химия" | Способ получения мономеров |
| US5466877A (en) * | 1994-03-15 | 1995-11-14 | Minnesota Mining And Manufacturing Company | Process for converting perfluorinated esters to perfluorinated acyl fluorides and/or ketones |
Non-Patent Citations (1)
| Title |
|---|
| K. Murata et al. The Termal Decomposition of Perfluoroester. J. Am. Chem. Soc. 1998, v.120, n. 28, p. 7117-7118. * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU6866000A (en) | 2001-03-26 |
| US6833477B2 (en) | 2004-12-21 |
| DE60014673T2 (de) | 2005-02-17 |
| EP1208075A1 (en) | 2002-05-29 |
| CA2381351C (en) | 2009-11-17 |
| ATE278657T1 (de) | 2004-10-15 |
| US20020107358A1 (en) | 2002-08-08 |
| CN1371353A (zh) | 2002-09-25 |
| WO2001016085A1 (en) | 2001-03-08 |
| EP1208075B1 (en) | 2004-10-06 |
| JP4626118B2 (ja) | 2011-02-02 |
| KR100704527B1 (ko) | 2007-04-10 |
| DE60014673D1 (de) | 2004-11-11 |
| JP2003508374A (ja) | 2003-03-04 |
| CA2381351A1 (en) | 2001-03-08 |
| KR20020025244A (ko) | 2002-04-03 |
| CN1167662C (zh) | 2004-09-22 |
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| PD4A | Correction of name of patent owner |