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ES2687444T3 - Procedimiento para la preparación del 2,3,3,3-tetrafluoro-1-propeno - Google Patents

Procedimiento para la preparación del 2,3,3,3-tetrafluoro-1-propeno Download PDF

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Publication number
ES2687444T3
ES2687444T3 ES09725078.1T ES09725078T ES2687444T3 ES 2687444 T3 ES2687444 T3 ES 2687444T3 ES 09725078 T ES09725078 T ES 09725078T ES 2687444 T3 ES2687444 T3 ES 2687444T3
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Spain
Prior art keywords
tetrafluoro
propene
procedure
preparation
previous step
Prior art date
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Active
Application number
ES09725078.1T
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English (en)
Inventor
Michel Devic
Dominique Guillet
Emmanuel Guiraud
Laurent Wendlinger
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Arkema France SA
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Arkema France SA
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Publication of ES2687444T3 publication Critical patent/ES2687444T3/es
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C21/00—Acyclic unsaturated compounds containing halogen atoms
    • C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
    • C07C21/18—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds 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
    • B01J23/70—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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • B01J37/0207—Pretreatment of the support
    • 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
    • C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00—Preparation of halogenated hydrocarbons
    • C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
    • C07C17/354—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by hydrogenation
    • 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
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04—Alumina
    • 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
    • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J35/61—Surface area
    • B01J35/613—10-100 m2/g
    • 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
    • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J35/63—Pore volume
    • B01J35/633—Pore volume less than 0.5 ml/g

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)

Abstract

Procedimiento continuo en fase de gas de preparación de 2,3,3,3-tetrafluoro-1-propeno que comprende las siguientes etapas: (i) hidrogenación de hexafluoropropileno en 1,1,1,2,3,3-hexafluoropropano; (ii) deshidrofluoración del 1,1,1,2,3,3-hexafluoropropano obtenido en la etapa anterior en 1,2,3,3,3- pentafluoropropeno-1, en presencia de hidrógeno; (iii) hidrogenación del 1,2,3,3,3-pentafluoropropeno-1 obtenido en la etapa anterior en 1,1,1,2,3- pentafluoropropano; (iv) deshidrofluoración del 1,1,1,2,3-pentafluoropropano obtenido en la etapa anterior en 2,3,3,3-tetrafluoro-1- propeno.

Description

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Claims (1)

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ES09725078.1T 2008-03-28 2009-03-27 Procedimiento para la preparación del 2,3,3,3-tetrafluoro-1-propeno Active ES2687444T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0801727A FR2929272B1 (fr) 2008-03-28 2008-03-28 Procede pour la preparation du 2,3,3,3-tetrafluoro-1-propene
FR0801727 2008-03-28
PCT/IB2009/005095 WO2009118632A1 (fr) 2008-03-28 2009-03-27 Procede pour la preparation du 2,3,3,3-tetrafluoro-1-propene

Publications (1)

Publication Number Publication Date
ES2687444T3 true ES2687444T3 (es) 2018-10-25

Family

ID=39876510

Family Applications (1)

Application Number Title Priority Date Filing Date
ES09725078.1T Active ES2687444T3 (es) 2008-03-28 2009-03-27 Procedimiento para la preparación del 2,3,3,3-tetrafluoro-1-propeno

Country Status (8)

Country Link
US (1) US8329964B2 (es)
EP (2) EP2271604B1 (es)
JP (2) JP2011515457A (es)
CN (2) CN105016964A (es)
ES (1) ES2687444T3 (es)
FR (1) FR2929272B1 (es)
PL (1) PL2271604T3 (es)
WO (1) WO2009118632A1 (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8766020B2 (en) * 2008-07-31 2014-07-01 Honeywell International Inc. Process for producing 2,3,3,3-tetrafluoropropene
US8710282B2 (en) 2008-03-14 2014-04-29 Honeywell International Inc. Integrated process for the manufacture of fluorinated olefins
GB0808836D0 (en) * 2008-05-15 2008-06-18 Ineos Fluor Ltd Process
FR2935703B1 (fr) * 2008-09-11 2010-09-03 Arkema France Procede de preparation de composes fluores.
FR2948361B1 (fr) 2009-07-23 2011-08-05 Arkema France Procede de preparation de composes fluores
FR2948362B1 (fr) * 2009-07-23 2012-03-23 Arkema France Procede de preparation de composes fluores
US8158549B2 (en) * 2009-09-04 2012-04-17 Honeywell International Inc. Catalysts for fluoroolefins hydrogenation
CN102267869A (zh) * 2011-05-27 2011-12-07 山东东岳高分子材料有限公司 2,3,3,3-四氟丙烯的合成方法
GB201207666D0 (en) * 2012-05-02 2012-06-13 Mexichem Amanco Holding Sa Process
US9290424B2 (en) 2013-03-14 2016-03-22 Honeywell International Inc. Processes for the hydrogenation of halogenated alkenes and the manufacture of fluorinated olefins
CN103449960B (zh) * 2013-08-06 2016-01-20 巨化集团技术中心 一种1,1,1,2,3-五氟丙烷的制备方法
JP6328589B2 (ja) 2015-05-29 2018-05-23 ダイキン工業株式会社 含フッ素オレフィンの製造方法
CN104945221B (zh) * 2015-06-11 2017-07-18 浙江衢州巨新氟化工有限公司 一种联产2,3,3,3‑四氟丙烯和1,3,3,3‑四氟丙烯的方法
CN105130743B (zh) * 2015-07-30 2017-05-24 浙江衢州巨新氟化工有限公司 一种 2,3,3,3‑四氟丙烯的生产方法
KR20160017661A (ko) 2016-01-29 2016-02-16 한국과학기술연구원 헥사플루오로프로필렌으로부터 2,3,3,3-테트라플루오로프로펜과 1,3,3,3-테트라플루오로프로펜의 제조방법
KR101914236B1 (ko) 2017-01-11 2018-12-28 한국과학기술연구원 1,2,3,3,3-펜타플루오로프로펜 제조방법
KR101992230B1 (ko) 2017-08-08 2019-06-25 (주)후성 기상 촉매를 이용한 1,1,1-트리플루오로-2-클로로프로펜과 1,1,1,2-테트라플루오로프로펜의 동시 제조 방법
CN112313199A (zh) 2018-06-06 2021-02-02 霍尼韦尔国际公司 用于HCFC-244bb的脱氯化氢以制备HFO-1234yf的方法
WO2021093029A1 (en) 2019-11-13 2021-05-20 Fujian Yongjing Technology Co., Ltd New process for synthesis of 2,3,3,3-tetrafluoropropene (1234yf) and 2,3-dichloro-1,1,1-trifluoropropane (243db)

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4902838A (en) 1988-12-28 1990-02-20 E. I. Du Pont De Nemours And Company Isomerization of saturated fluorohydrocarbons
FR2669022B1 (fr) 1990-11-13 1992-12-31 Atochem Procede de fabrication du tetrafluoro-1,1,1,2-ethane.
WO1993025510A1 (en) 1992-06-05 1993-12-23 Daikin Industries, Ltd. Processes for producing 1,1,1,2,3-pentafluoropropene and producing 1,1,1,2,3-pentafluoropropane
US5396000A (en) 1993-05-24 1995-03-07 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,1,1,2,3,-pentafluoropropane
JP3543863B2 (ja) 1994-12-16 2004-07-21 ダイキン工業株式会社 １，１，１，２，３，３−ヘキサフルオロプロパンの製造方法
US6369284B1 (en) * 1997-01-31 2002-04-09 E. I. Du Pont De Nemours And Company Catalytic manufacture of pentafluoropropenes
CA2628463C (en) 2005-11-03 2014-07-08 Honeywell International Inc. Method for producing fluorinated organic compounds
US7560602B2 (en) 2005-11-03 2009-07-14 Honeywell International Inc. Process for manufacture of fluorinated olefins
WO2007117391A1 (en) * 2006-03-31 2007-10-18 E.I. Du Pont De Nemours And Company Coproduction of hydrofluoroolefins
WO2008002500A1 (en) * 2006-06-27 2008-01-03 E. I. Du Pont De Nemours And Company Tetrafluoropropene production processes
US7833434B2 (en) 2006-06-27 2010-11-16 E. I. Du Pont De Nemours And Company Tetrafluoropropene production processes
US7485760B2 (en) * 2006-08-24 2009-02-03 Honeywell International Inc. Integrated HFC trans-1234ze manufacture process
EP2066605B1 (en) * 2006-09-05 2013-12-25 E.I. Du Pont De Nemours And Company Process to manufacture 2,3,3,3-tetrafluoropropene
ES2590683T3 (es) * 2007-12-27 2016-11-23 Arkema France Procedimiento para producir 1,1,1,2-tetrafluoropropeno

Also Published As

Publication number Publication date
PL2271604T3 (pl) 2018-11-30
JP2011515457A (ja) 2011-05-19
CN105016964A (zh) 2015-11-04
JP5947337B2 (ja) 2016-07-06
CN101980994A (zh) 2011-02-23
US8329964B2 (en) 2012-12-11
WO2009118632A1 (fr) 2009-10-01
EP2271604A1 (fr) 2011-01-12
JP2014185168A (ja) 2014-10-02
US20100305370A1 (en) 2010-12-02
FR2929272B1 (fr) 2010-04-09
EP2271604B1 (fr) 2018-06-27
FR2929272A1 (fr) 2009-10-02
EP3398924A1 (fr) 2018-11-07

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