JP2001322955A5 - - Google Patents

Download PDF

Info

Publication number
JP2001322955A5
JP2001322955A5 JP2000143022A JP2000143022A JP2001322955A5 JP 2001322955 A5 JP2001322955 A5 JP 2001322955A5 JP 2000143022 A JP2000143022 A JP 2000143022A JP 2000143022 A JP2000143022 A JP 2000143022A JP 2001322955 A5 JP2001322955 A5 JP 2001322955A5
Authority
JP
Japan
Prior art keywords
alkali metal
metal hydroxide
trifluoropropene
aqueous solution
hydroxide
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP2000143022A
Other languages
Japanese (ja)
Other versions
JP2001322955A (en
Filing date
Publication date
Application filed filed Critical
Priority to JP2000143022A priority Critical patent/JP2001322955A/en
Priority claimed from JP2000143022A external-priority patent/JP2001322955A/en
Publication of JP2001322955A publication Critical patent/JP2001322955A/en
Publication of JP2001322955A5 publication Critical patent/JP2001322955A5/ja
Pending legal-status Critical Current

Links

Description

【特許請求の範囲】
【請求項1】 1,2−ジブロモ−3,3,3−トリフルオロプロパンとアルカリ金属水酸化物とを水を溶媒として30〜130℃で反応させることを特徴とする2−ブロモ−3,3,3−トリフルオロプロペンの製造方法。
【請求項2】 アルカリ金属水酸化物の水溶液を30〜130℃に加熱し攪拌しながら、該水溶液に1,2−ジブロモ−3,3,3−トリフルオロプロパンを滴下して反応させつつ蒸留精製することにより、2−ブロモ−3,3,3−トリフルオロプロペンを得ることを特徴とする2−ブロモ−3,3,3−トリフルオロプロペンの製造方法。
【請求項3】 反応温度を、40〜90℃の範囲内とする請求項1または2記載の製造方法。
【請求項4】 アルカリ金属水酸化物を、水酸化ナトリウムまたは水酸化カリウムのいずれかとする請求項1または2記載の製造方法。
【請求項5】 アルカリ金属水酸化物の水溶液濃度を、5〜30重量%とする請求項1または2記載の製造方法。
[Claims]
1. A method according to claim 1, wherein 1,2-dibromo-3,3,3-trifluoropropane is reacted with an alkali metal hydroxide at 30 to 130 ° C. using water as a solvent. A method for producing 3,3-trifluoropropene.
2. An aqueous solution of an alkali metal hydroxide is heated to 30 to 130 ° C. and stirred, and 1,2-dibromo-3,3,3-trifluoropropane is added dropwise to the aqueous solution to carry out distillation while reacting. A method for producing 2-bromo-3,3,3-trifluoropropene, comprising obtaining 2-bromo-3,3,3-trifluoropropene by purification.
3. The method according to claim 1 , wherein the reaction temperature is in the range of 40 to 90 ° C.
The wherein the alkali metal hydroxide method according to claim 1 or 2, wherein either the sodium hydroxide or potassium hydroxide.
5. The method according to claim 1 , wherein the concentration of the aqueous solution of the alkali metal hydroxide is 5 to 30% by weight.

JP2000143022A 2000-05-16 2000-05-16 Method for producing 2-bromo-3,3,3-trifluoropropene Pending JP2001322955A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000143022A JP2001322955A (en) 2000-05-16 2000-05-16 Method for producing 2-bromo-3,3,3-trifluoropropene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000143022A JP2001322955A (en) 2000-05-16 2000-05-16 Method for producing 2-bromo-3,3,3-trifluoropropene

Publications (2)

Publication Number Publication Date
JP2001322955A JP2001322955A (en) 2001-11-20
JP2001322955A5 true JP2001322955A5 (en) 2007-04-19

Family

ID=18649894

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000143022A Pending JP2001322955A (en) 2000-05-16 2000-05-16 Method for producing 2-bromo-3,3,3-trifluoropropene

Country Status (1)

Country Link
JP (1) JP2001322955A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102482180B (en) * 2009-08-31 2014-08-27 住友化学株式会社 Method for producing 1,1,3-trichloro-1-propene
CN102206134B (en) * 2011-04-02 2014-02-05 西安近代化学研究所 Preparation method of 2-bromine-3,3,3-trifluoropropene
JP6183370B2 (en) * 2012-09-21 2017-08-23 セントラル硝子株式会社 Process for producing 1,2-dichloro-3,3,3-trifluoropropene
US8877988B2 (en) 2012-12-21 2014-11-04 Honeywell International Inc. Synthesis of 1-BROM0-3,3,3-trifluoropropene
WO2023176433A1 (en) * 2022-03-16 2023-09-21 株式会社レゾナック Fluoroalkene storage method
WO2023176434A1 (en) * 2022-03-16 2023-09-21 株式会社レゾナック Method for storing fluoroalkene

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5921648A (en) * 1982-07-29 1984-02-03 Sagami Chem Res Center Methacrylic acid ester containing fluorine

Similar Documents

Publication Publication Date Title
WO2008030439A3 (en) Dehydrofluorination process to manufacture hydrofluoroolefins
WO2006063241A3 (en) Direct one-step synthesis from cf3-i
WO2006055748A3 (en) Method for the preparation of sevoflurane
JP2005527623A5 (en)
JP2001322955A5 (en)
WO2002055459A3 (en) Method of making hydrofluorocarbons and hydrochlorofluorocarbons
MXPA04005141A (en) Process for the manufacture of methyl cellulose ether.
JP2006514107A5 (en)
JP2008143794A5 (en)
US20140228417A1 (en) Process and intermediates for the preparation of substituted 2-arylthiazole carboxylic acids
CN104193664B (en) A kind of synthetic method of imrecoxib
JP2001206881A5 (en)
CN105859540B (en) A kind of chloroacetic synthesis and production process of difluoro
CA2397497A1 (en) Process for the preparation of 5-carboxyphthalide and its use for the production of citalopram
CN112939893B (en) Synthesis method of 4- (4-aminophenyl) -3-morpholinone
JP3078631B2 (en) Method for producing chloromethylhalogenopyridines
KR890005045A (en) Oxethylmercapto benzaldehyde and its oxidation product
JP2009242370A (en) Method for producing toluidine compound
NZ596447A (en) Process for the preparation of a iodinating agent
EE200200417A (en) Process for the preparation of 6- (4-chlorophenyl) -2,2-dimethyl-7-phenyl-2,3-dihydro-1H-pyrrolizin-5-ylacetic acid
JP5200428B2 (en) Method for producing tetrahydropyran-4-one
JPS6133A (en) Production of methallyl alcohol
JP2007519660A5 (en)
CN104478742A (en) Fluoro compound and preparation method thereof
JP2006520762A5 (en)