RU2005107804A - Способы получения 2-хлор-1,1,1,2,3,3,3-гептафторпропана, гексафторпропена и 1,1,1,2,3,3,3-гептафторпропана - Google Patents
Способы получения 2-хлор-1,1,1,2,3,3,3-гептафторпропана, гексафторпропена и 1,1,1,2,3,3,3-гептафторпропана Download PDFInfo
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- RU2005107804A RU2005107804A RU2005107804/04A RU2005107804A RU2005107804A RU 2005107804 A RU2005107804 A RU 2005107804A RU 2005107804/04 A RU2005107804/04 A RU 2005107804/04A RU 2005107804 A RU2005107804 A RU 2005107804A RU 2005107804 A RU2005107804 A RU 2005107804A
- Authority
- RU
- Russia
- Prior art keywords
- chromium
- atoms
- cclfcf
- nickel
- alpha
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 5
- KJGXPVLCSICDQG-UHFFFAOYSA-N 2-chloro-1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)(Cl)C(F)(F)F KJGXPVLCSICDQG-UHFFFAOYSA-N 0.000 title claims 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 title 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 8
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims 4
- 229910000423 chromium oxide Inorganic materials 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 229910052759 nickel Inorganic materials 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000000460 chlorine Substances 0.000 claims 3
- 229910017052 cobalt Inorganic materials 0.000 claims 3
- 239000010941 cobalt Substances 0.000 claims 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 3
- 239000013078 crystal Substances 0.000 claims 3
- 150000008282 halocarbons Chemical class 0.000 claims 3
- 239000000543 intermediate Substances 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052804 chromium Inorganic materials 0.000 claims 1
- 239000011651 chromium Substances 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims 1
- 238000005984 hydrogenation reaction Methods 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 239000012808 vapor phase Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C19/00—Acyclic saturated compounds containing halogen atoms
- C07C19/08—Acyclic saturated compounds containing halogen atoms containing fluorine
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/24—Chromium, molybdenum or tungsten
- B01J23/26—Chromium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/86—Chromium
- B01J23/866—Nickel and chromium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/70—Catalysts, in general, characterised by their form or physical properties characterised by their crystalline properties, e.g. semi-crystalline
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/22—Halogenating
- B01J37/26—Fluorinating
-
- 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
- C07C17/093—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
- C07C17/21—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms with simultaneous increase of the number of halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/23—Preparation of halogenated hydrocarbons by dehalogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0236—Drying, e.g. preparing a suspension, adding a soluble salt and drying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/03—Precipitation; Co-precipitation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Claims (3)
1. Способ получения 2-хлор-1,1,1,2,3,3,3-гептафторпропана, включающий:
(а) контактирование смеси, содержащей фтороводород, хлор и, по меньшей мере, одно исходное вещество, выбранное из группы, состоящей из галогенпропенов формулы СХ3CCl=СХ2 и галогенпропанов формулы СХ3CClYCX3, где каждый Х независимо выбран из группы, состоящей из F и Cl, и Y выбран из группы, состоящей из Н, Cl и F, при условии, что число Х и Y, которые являются F, в целом не более шести, с катализатором хлорфторирования в зоне реакции с получением продукта в виде смеси, содержащей CF3CClFCF3, HCl, HF и недостаточно фторированные галогенированные углеводородные промежуточные соединения,
где указанный катализатор хлорфторирования содержит, по меньшей мере, один содержащий хром компонент, выбранный из (i) кристаллического альфа-оксида хрома, где, по меньшей мере, 0,05 атом. % атомов хрома в кристаллической решетке альфа-оксида хрома заменено на никель, трехвалентный кобальт или как на никель, так и на трехвалентный кобальт, при условии, что не более 2 атом. % атомов хрома в кристаллической решетке альфа-оксида хрома заменено на никель, и что общее количество атомов хрома в кристаллической решетке альфа-оксида хрома, которые заменены никелем и трехвалентным кобальтом, составляет не более 6 атом. %, и (ii) фторированного кристаллического оксида (i).
2. Способ по п.1, дополнительно включающий:
(b) разделение продукта со стадии (а) с выделением CF3CClFCF3 как продукта и с получением недостаточно фторированных галогенированных углеводородных промежуточных соединений; и
(с) возвращение недостаточно фторированных галогенированных углеводородных промежуточных соединений, полученных на стадии (b), обратно на стадию (а) в зону реакции.
3. Способ получения смеси CF3CHFCF3 и CF2=CFCF3 путем взаимодействия исходной смеси, содержащей CF3CClFCF3 и водород в паровой фазе при повышенной температуре, возможно, в присутствии катализатора гидрогенизации, отличающийся тем, что CF3CClFCF3 получают по способу по п.1.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40522202P | 2002-08-22 | 2002-08-22 | |
US60/405,222 | 2002-08-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2005107804A true RU2005107804A (ru) | 2005-08-27 |
RU2326859C2 RU2326859C2 (ru) | 2008-06-20 |
Family
ID=31946829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2005107804/04A RU2326859C2 (ru) | 2002-08-22 | 2003-08-21 | Способы получения 2-хлор-1,1,1,2,3,3,3-гептафторпропана, гексафторпропена и 1,1,1,2,3,3,3-гептафторпропана |
Country Status (8)
Country | Link |
---|---|
US (1) | US7129383B2 (ru) |
EP (1) | EP1539661B1 (ru) |
JP (1) | JP2005536540A (ru) |
CN (1) | CN1279007C (ru) |
AU (1) | AU2003265595A1 (ru) |
DE (1) | DE60323994D1 (ru) |
RU (1) | RU2326859C2 (ru) |
WO (1) | WO2004018397A1 (ru) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2003265592A1 (en) * | 2002-08-22 | 2004-03-11 | E.I. Du Pont De Nemours And Company | Nickel-substituted and mixed nickel-and-cobalt-substituted chromium oxide compositions, their preparation, and their use as catalysts and catalyst precursors |
EP1539347B1 (en) | 2002-08-22 | 2012-06-27 | E.I. Du Pont De Nemours And Company | Cobalt substituted chromium oxide compositions, their preparation and their use as catalysts and catalyst precursors |
US7279451B2 (en) * | 2002-10-25 | 2007-10-09 | Honeywell International Inc. | Compositions containing fluorine substituted olefins |
US20050020863A1 (en) * | 2003-07-25 | 2005-01-27 | Honeywell International Inc. | Method of making fluorinated propanes |
GB0507139D0 (en) * | 2005-04-08 | 2005-05-18 | Ineos Fluor Holdings Ltd | Catalyst |
TW201742908A (zh) * | 2005-06-24 | 2017-12-16 | 哈尼威爾國際公司 | 含有經氟取代之烯烴之組合物 |
WO2007019355A1 (en) * | 2005-08-05 | 2007-02-15 | E. I. Du Pont De Nemours And Company | Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 2,3,3,3-tetrafluoropropene |
US8053611B2 (en) * | 2005-08-05 | 2011-11-08 | E. I. Du Pont De Nemours And Company | Process or the preparation of 1,1,1,3,3,3-hexafluoro-propane and at least one of 1,1,1,2,3,3-hexafluoropropane, hexafluoropropane and 1,1,1,2,3,3,3-heptafluoropropane |
WO2007019357A1 (en) * | 2005-08-05 | 2007-02-15 | E. I. Du Pont De Nemours And Company | Process for the preparation of 1,1,1,3,3-pentafluoropropane and/or 1,1,1,3,3,3,-hexafluoropropane |
US7663007B2 (en) | 2005-08-05 | 2010-02-16 | E.I. Du Pont De Nemours And Company | Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 1,1,3,3,3-pentafluoropropene |
WO2007019356A2 (en) * | 2005-08-05 | 2007-02-15 | E. I. Du Pont De Nemours And Company | Copper-substituted chromium oxide compositions, their preparation, and their use as catalysts and catalyst precursors |
US8017817B2 (en) * | 2005-08-05 | 2011-09-13 | E.I. Du Pont De Nemours And Company | Process for the preparation of 1,1,3,3,3-pentafluoropropene and 1,2,3,3,3-pentafluoropropene |
WO2007019353A1 (en) * | 2005-08-05 | 2007-02-15 | E. I. Du Pont De Nemours And Company | Process for the preparation of 1,1,1,3,3-pentafluoropropane and 1,1,1,2,3-pentafluoropropane |
US7718319B2 (en) | 2006-09-25 | 2010-05-18 | Board Of Regents, The University Of Texas System | Cation-substituted spinel oxide and oxyfluoride cathodes for lithium ion batteries |
US20080207962A1 (en) * | 2007-02-23 | 2008-08-28 | Velliyur Nott Mallikarjuna Rao | Compositions containing chromium, oxygen, and at least two modifier metals selected the group consisting of gold, silver, and palladium, their preparation, and their use as catalysts and catalyst precursors |
US20080207964A1 (en) * | 2007-02-23 | 2008-08-28 | Velliyur Nott Mallikarjuna Rao | Compositions containing chromium, oxygen and gold, their preparation, and their use as catalysts and catalyst precursors |
US20080207963A1 (en) * | 2007-02-23 | 2008-08-28 | Velliyur Nott Mallikarjuna Rao | Preparation of composition containing chromium, oxygen, and either silver or palladium, and their use as catalysts and catalyst precursors |
GB0721991D0 (en) | 2007-11-09 | 2007-12-19 | Ineos Fluor Holdings Ltd | Preparation method |
CN103242132A (zh) * | 2012-02-01 | 2013-08-14 | 中化蓝天集团有限公司 | 一种制备1,1,1,2,3,3,3-七氟丙烷的方法 |
CN103319302B (zh) * | 2013-06-28 | 2015-07-01 | 南京信息工程大学 | 一种七氯丙烷的制备方法 |
EP3153491A4 (en) * | 2014-06-06 | 2017-12-13 | Asahi Glass Company, Limited | Method for producing 1,1-dichloro-3,3,3-trifluoropropane |
CN112125777B (zh) | 2020-08-27 | 2022-06-03 | 浙江衢化氟化学有限公司 | 一种联产氢氟烃的方法 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
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GB902590A (en) | 1960-03-22 | 1962-08-01 | Allied Chem | Production of heptafluoropropane |
US3878257A (en) * | 1973-08-10 | 1975-04-15 | Du Pont | Catalytic conversion of 1,1,2-trichlorotrifluoropropene-1 to 2-chloropentafluoropropene |
US3865885A (en) * | 1973-08-10 | 1975-02-11 | Du Pont | Catalytic chlorofluorination of isopropyl fluoride to 1,1,2-trichlorotrifluoropropene-1 |
EP0002098B1 (en) | 1977-11-10 | 1981-08-12 | E.I. Du Pont De Nemours And Company | Removal of perfluoroisobutylene |
US4843181A (en) * | 1987-10-22 | 1989-06-27 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,1,1-trifluorodichloroethane and 1,1,1,2-tetrafluorochloroethane |
US5364992A (en) * | 1989-10-10 | 1994-11-15 | E. I. Du Pont De Nemours And Company | Halocarbon hydrogenolysis |
US5068472A (en) * | 1989-12-19 | 1991-11-26 | E. I. Du Pont De Nemours And Company | Multistep synthesis of hexafluoropropylene |
US5057634A (en) * | 1989-12-19 | 1991-10-15 | E. I. Du Pont De Nemours And Company | Multistep synthesis of hexafluoropropylene |
US5043491A (en) * | 1989-12-19 | 1991-08-27 | E. I. Du Pont De Nemours And Company | Multistep synthesis of hexafluoropropylene |
FR2684567B1 (fr) | 1991-12-09 | 1994-11-04 | Atochem | Catalyseurs massiques a base d'oxydes de chrome et de nickel, et leur application a la fluoration d'hydrocarbures halogenes. |
FR2713633B1 (fr) | 1993-12-09 | 1996-01-19 | Atochem Elf Sa | Fluoration en phase gazeuse au moyen de catalyseurs cristallisés. |
EP1066230B1 (en) | 1998-04-03 | 2003-09-10 | E.I. Du Pont De Nemours And Company | Processes for the purification and use of 2-chloro-1,1,1,2,3,3,3-heptafluoropropane and azeotropes thereof with hf |
DE69910995T2 (de) * | 1998-04-03 | 2004-07-22 | E.I. Du Pont De Nemours And Co., Wilmington | Verfahren zur herstellung von fluorkohlenwasserstoffen |
US6018083A (en) * | 1998-04-03 | 2000-01-25 | E. I. Du Pont De Nemours And Company | Process for the production of fluorocarbons |
EP1539347B1 (en) | 2002-08-22 | 2012-06-27 | E.I. Du Pont De Nemours And Company | Cobalt substituted chromium oxide compositions, their preparation and their use as catalysts and catalyst precursors |
AU2003265592A1 (en) | 2002-08-22 | 2004-03-11 | E.I. Du Pont De Nemours And Company | Nickel-substituted and mixed nickel-and-cobalt-substituted chromium oxide compositions, their preparation, and their use as catalysts and catalyst precursors |
-
2003
- 2003-08-21 EP EP03793285A patent/EP1539661B1/en not_active Expired - Lifetime
- 2003-08-21 WO PCT/US2003/026331 patent/WO2004018397A1/en active Application Filing
- 2003-08-21 AU AU2003265595A patent/AU2003265595A1/en not_active Abandoned
- 2003-08-21 RU RU2005107804/04A patent/RU2326859C2/ru not_active IP Right Cessation
- 2003-08-21 US US10/523,223 patent/US7129383B2/en not_active Expired - Fee Related
- 2003-08-21 DE DE60323994T patent/DE60323994D1/de not_active Expired - Lifetime
- 2003-08-21 JP JP2004529846A patent/JP2005536540A/ja not_active Abandoned
- 2003-08-21 CN CN03819934.3A patent/CN1279007C/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN1279007C (zh) | 2006-10-11 |
EP1539661A1 (en) | 2005-06-15 |
CN1678551A (zh) | 2005-10-05 |
RU2326859C2 (ru) | 2008-06-20 |
WO2004018397A1 (en) | 2004-03-04 |
JP2005536540A (ja) | 2005-12-02 |
DE60323994D1 (de) | 2008-11-20 |
AU2003265595A1 (en) | 2004-03-11 |
US20050222471A1 (en) | 2005-10-06 |
US7129383B2 (en) | 2006-10-31 |
EP1539661B1 (en) | 2008-10-08 |
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