MX2013007757A - E-1-cloro-3,3,3-trifluoropropeno de alta pureza y metodos para elaborar el mismo. - Google Patents

E-1-cloro-3,3,3-trifluoropropeno de alta pureza y metodos para elaborar el mismo.

Info

Publication number
MX2013007757A
MX2013007757A MX2013007757A MX2013007757A MX2013007757A MX 2013007757 A MX2013007757 A MX 2013007757A MX 2013007757 A MX2013007757 A MX 2013007757A MX 2013007757 A MX2013007757 A MX 2013007757A MX 2013007757 A MX2013007757 A MX 2013007757A
Authority
MX
Mexico
Prior art keywords
methods
trifluoropropene
chloro
high purity
making
Prior art date
Application number
MX2013007757A
Other languages
English (en)
Other versions
MX358513B (es
Inventor
Hsueh Sung Tung
Rajiv Ratna Singh
Ian Shankland
Konstantin A Pokrovski
Original Assignee
Honeywell Int Inc
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.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46381341&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MX2013007757(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Honeywell Int Inc filed Critical Honeywell Int Inc
Publication of MX2013007757A publication Critical patent/MX2013007757A/es
Publication of MX358513B publication Critical patent/MX358513B/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/361Preparation of halogenated hydrocarbons by reactions involving a decrease in the number of carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/20Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
    • C07C17/202Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
    • C07C17/206Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/25Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/38Separation; Purification; Stabilisation; Use of additives
    • C07C17/383Separation; Purification; Stabilisation; Use of additives by distillation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C21/00Acyclic unsaturated compounds containing halogen atoms
    • C07C21/02Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
    • C07C21/18Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds containing fluorine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/09Geometrical isomers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

La presente invención describe E-1-cloro-3,3,3-trifluoropropeno de alta pureza (1233zd(E)) y métodos para producir el mismo. Más específicamente, la presente invención describe los métodos para elaborar 1233zd(E) esencialmente libres de impurezas tóxicas (por ejemplo, 2-cloro-3,3,3-trifluoropropeno (1233xf), clorotetrafluoro-propeno (1224) y 3,3,3-trifluoropropino). La presente invención además proporciona métodos para elaborar 1233zd(E) de alta pureza con una concentración de 1233xf y 1224 en o debajo de 200 partes por millón (ppm) e impurezas de 3,3,3-trifluoropropino en o debajo de 20 ppm. La formación de impurezas de 1233xf puede evitarse si el 1,1,1,3,3-pentacloropropa no puro se utiliza como un material de partida. También se establece que la formación de 1233xf se evita si se utiliza un proceso de fabricación de fases líquidas.
MX2013007757A 2011-01-04 2012-01-03 E-1-cloro-3,3,3-trifluoropropeno de alta pureza y métodos para elaborar el mismo. MX358513B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12/984,024 US9156752B2 (en) 2011-01-04 2011-01-04 High purity E-1-chloro-3,3,3-trifluoropropene and methods of making the same
PCT/US2012/020035 WO2012094288A2 (en) 2011-01-04 2012-01-03 High purity e-1-chloro-3,3,3-trifluoropropene and methods of making the same

Publications (2)

Publication Number Publication Date
MX2013007757A true MX2013007757A (es) 2013-08-15
MX358513B MX358513B (es) 2018-08-24

Family

ID=46381341

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2013007757A MX358513B (es) 2011-01-04 2012-01-03 E-1-cloro-3,3,3-trifluoropropeno de alta pureza y métodos para elaborar el mismo.

Country Status (8)

Country Link
US (2) US9156752B2 (es)
EP (1) EP2661419B1 (es)
JP (3) JP6225028B2 (es)
KR (1) KR101990066B1 (es)
CN (1) CN103402953B (es)
ES (1) ES2549641T3 (es)
MX (1) MX358513B (es)
WO (1) WO2012094288A2 (es)

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US9272968B2 (en) * 2013-03-14 2016-03-01 Honeywell International Inc. Process to suppress the formation of 3,3,3-trifluoropropyne in fluorocarbon manufacture
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FR3036398B1 (fr) * 2015-05-22 2019-05-03 Arkema France Compositions a base de 1,1,3,3-tetrachloropropene
JP6826280B2 (ja) * 2016-01-15 2021-02-03 セントラル硝子株式会社 トランス−1−クロロ−3,3,3−トリフルオロプロペンの製造方法
US10029964B2 (en) * 2016-08-30 2018-07-24 Honeywell International Inc. Azeotropic or azeotrope-like compositions of 3,3,3-trifluoropropyne and water
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FR3081158B1 (fr) * 2018-05-16 2020-07-31 Arkema France Procede de production du 1-chloro-3,3,3-trifluoropropene.
FR3083232B1 (fr) 2018-06-27 2021-11-12 Arkema France Procede de production du 1-chloro-3,3,3-trifluoropropene
FR3086287B1 (fr) 2018-09-26 2020-09-18 Arkema France Stabilisation du 1-chloro-3,3,3-trifluoropropene
CN113039172A (zh) * 2018-11-15 2021-06-25 阿科玛股份有限公司 将含氢氯氟烯烃的粗制流中和并从中除去hf的方法
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Also Published As

Publication number Publication date
EP2661419A4 (en) 2014-07-02
CN103402953B (zh) 2015-08-12
KR101990066B1 (ko) 2019-06-17
WO2012094288A3 (en) 2012-08-30
US9156752B2 (en) 2015-10-13
WO2012094288A2 (en) 2012-07-12
JP6225028B2 (ja) 2017-11-01
JP2016164172A (ja) 2016-09-08
CN103402953A (zh) 2013-11-20
US9862662B2 (en) 2018-01-09
US20160002128A1 (en) 2016-01-07
EP2661419A2 (en) 2013-11-13
ES2549641T3 (es) 2015-10-30
US20120172636A1 (en) 2012-07-05
JP2014509310A (ja) 2014-04-17
JP6527575B2 (ja) 2019-06-05
EP2661419B1 (en) 2015-07-29
JP2018070656A (ja) 2018-05-10
KR20180120276A (ko) 2018-11-05
MX358513B (es) 2018-08-24

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