MX358513B - E-1-cloro-3,3,3-trifluoropropeno de alta pureza y métodos para elaborar el mismo. - Google Patents

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

Info

Publication number
MX358513B
MX358513B MX2013007757A MX2013007757A MX358513B MX 358513 B MX358513 B MX 358513B MX 2013007757 A MX2013007757 A MX 2013007757A MX 2013007757 A MX2013007757 A MX 2013007757A MX 358513 B MX358513 B MX 358513B
Authority
MX
Mexico
Prior art keywords
methods
trifluoropropene
chloro
high purity
making
Prior art date
Application number
MX2013007757A
Other languages
English (en)
Other versions
MX2013007757A (es
Inventor
Sung Tung Hsueh
Ratna Singh Rajiv
Shankland Ian
A Pokrovski Konstantin
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=MX358513(B) "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

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00—Preparation of halogenated hydrocarbons
    • C07C17/361—Preparation of halogenated hydrocarbons by reactions involving a decrease in the number of carbon atoms
    • 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
    • C07C17/25—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
    • C07C17/38—Separation; Purification; Stabilisation; Use of additives
    • C07C17/383—Separation; Purification; Stabilisation; Use of additives by distillation
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/09—Geometrical 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 MX2013007757A (es) 2013-08-15
MX358513B true 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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US9000240B2 (en) 2011-05-19 2015-04-07 Honeywell International Inc. Integrated process for the production of 1-chloro-3,3,3-trifluoropropene
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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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US9255045B2 (en) 2014-01-13 2016-02-09 Arkema France E-1-chloro-3,3,3-trifluoropropene production process from 1,1,3,3-tetrachloropropene
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WO2016052562A1 (ja) * 2014-10-02 2016-04-07 セントラル硝子株式会社 ２－クロロ－１，３，３，３－テトラフルオロプロペン及び１－クロロ－３，３，３－トリフルオロプロペンを含有する共沸様組成物
FR3027304B1 (fr) * 2014-10-16 2018-02-23 Arkema France Compositions a base de 1,1,1,3,3-pentachloropropane
US9764998B2 (en) * 2015-05-12 2017-09-19 Honeywell International Inc. Process for making HCFO-1233zd
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
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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
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Also Published As

Publication number Publication date
US20160002128A1 (en) 2016-01-07
EP2661419B1 (en) 2015-07-29
WO2012094288A3 (en) 2012-08-30
US9862662B2 (en) 2018-01-09
MX2013007757A (es) 2013-08-15
JP2018070656A (ja) 2018-05-10
JP2016164172A (ja) 2016-09-08
CN103402953B (zh) 2015-08-12
US9156752B2 (en) 2015-10-13
WO2012094288A2 (en) 2012-07-12
JP2014509310A (ja) 2014-04-17
KR101990066B1 (ko) 2019-06-17
EP2661419A2 (en) 2013-11-13
JP6527575B2 (ja) 2019-06-05
JP6225028B2 (ja) 2017-11-01
US20120172636A1 (en) 2012-07-05
CN103402953A (zh) 2013-11-20
EP2661419A4 (en) 2014-07-02
KR20180120276A (ko) 2018-11-05
ES2549641T3 (es) 2015-10-30

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