JPS5690059A - Preparation of 2,3-dihalogeno-5-trifluoromethylpyridine - Google Patents

Preparation of 2,3-dihalogeno-5-trifluoromethylpyridine

Info

Publication number
JPS5690059A
JPS5690059A JP16789579A JP16789579A JPS5690059A JP S5690059 A JPS5690059 A JP S5690059A JP 16789579 A JP16789579 A JP 16789579A JP 16789579 A JP16789579 A JP 16789579A JP S5690059 A JPS5690059 A JP S5690059A
Authority
JP
Japan
Prior art keywords
trifluoromethylpyridine
halogeno
pyridone
trifluoromethyl
give
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
JP16789579A
Other languages
Japanese (ja)
Inventor
Ryuzo Nishiyama
Kanichi Fujikawa
Isao Yokomichi
Takahiro Haga
Kuniaki Hase
Hirohito Hayashi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ishihara Sangyo Kaisha Ltd
Original Assignee
Ishihara Sangyo Kaisha Ltd
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
Application filed by Ishihara Sangyo Kaisha Ltd filed Critical Ishihara Sangyo Kaisha Ltd
Priority to JP16789579A priority Critical patent/JPS5690059A/en
Publication of JPS5690059A publication Critical patent/JPS5690059A/en
Pending legal-status Critical Current

Links

Landscapes

  • Pyridine Compounds (AREA)

Abstract

PURPOSE: To obtain the titled compound in high yield in a few stages without problems of waste water treatment, by reacting a 2-halogeno-5-trifluoromethylpyridine with an alkaline substance, and halogenating the reaction product in two stages.
CONSTITUTION: A 2-halogeno-5-trifluoromethylpyridine is added to a solution in which an alkaline substance is dissolved in a solvent, and heated at 50W130°C to give 5-trifluoromethyl-2-pyridone. The resultant pyridone is then reacted with a relatively weak halogenating agent, e.g. chlorine gas or bromine, in the presence of a solvent at 0W100°C, preferably 20W60°C, to form a 3-halogeno-5-trifluoromethyl-2- pyridone, which is further reacted with a halogenating agent, e.g. thonyl chloride or phosphous oxybromide, at 20W150°C, preferably 50W100°C, to give the aimed compound. The reaction in the second stage can be carried out continuously without isolating the halogenation product obtained in the first stage.
COPYRIGHT: (C)1981,JPO&Japio
JP16789579A 1979-12-24 1979-12-24 Preparation of 2,3-dihalogeno-5-trifluoromethylpyridine Pending JPS5690059A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16789579A JPS5690059A (en) 1979-12-24 1979-12-24 Preparation of 2,3-dihalogeno-5-trifluoromethylpyridine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16789579A JPS5690059A (en) 1979-12-24 1979-12-24 Preparation of 2,3-dihalogeno-5-trifluoromethylpyridine

Publications (1)

Publication Number Publication Date
JPS5690059A true JPS5690059A (en) 1981-07-21

Family

ID=15858048

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16789579A Pending JPS5690059A (en) 1979-12-24 1979-12-24 Preparation of 2,3-dihalogeno-5-trifluoromethylpyridine

Country Status (1)

Country Link
JP (1) JPS5690059A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4490534A (en) * 1981-11-04 1984-12-25 Ishihara Sangyo Kaisha Ltd. Process for producing 3-chloro-5-trifluoromethylpyridines
EP0272824A2 (en) * 1986-12-24 1988-06-29 Imperial Chemical Industries Plc Chemical compounds
CN107652228A (en) * 2016-10-28 2018-02-02 广州南新制药有限公司 Anti- kidney fibrosis medicine 1(Substituted benzyl)The synthetic method of 5 trifluoromethyl 2 (1H) pyridonium salt hydrochlorates

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4490534A (en) * 1981-11-04 1984-12-25 Ishihara Sangyo Kaisha Ltd. Process for producing 3-chloro-5-trifluoromethylpyridines
EP0272824A2 (en) * 1986-12-24 1988-06-29 Imperial Chemical Industries Plc Chemical compounds
CN107652228A (en) * 2016-10-28 2018-02-02 广州南新制药有限公司 Anti- kidney fibrosis medicine 1(Substituted benzyl)The synthetic method of 5 trifluoromethyl 2 (1H) pyridonium salt hydrochlorates

Similar Documents

Publication Publication Date Title
JPS5687599A (en) E 55 22halogenovinyl arabinofuranosyluracil and its preparation
JPS5690059A (en) Preparation of 2,3-dihalogeno-5-trifluoromethylpyridine
JPS577438A (en) Production of acid chloride
JPS55108828A (en) Preparation of chlorination product and ethyl benzene
JPS57120545A (en) Preparation of alpha-chloroacetophenone
JPS5547651A (en) Production of sulfoxyimine
JPS5665838A (en) Preparation of beta-alkoxymethoxymethyl halide
JPS5764646A (en) Preparation of 2,6-dichloro-4-nitro-phenol
ES8406407A1 (en) Process for the preparation of 1,2-dichloroethane.
JPS5735556A (en) Preparation of guanidinomethylcyclohexanecarboxylic acid ester
JPS5690041A (en) Preparation of 2,6-dichloro-p-nitrophenol
JPS5419964A (en) Preparation of thiophene-substituted fatty acid halode
JPS57108024A (en) Preparation of 3-chlorobenzotrifluoride
JPS568457A (en) Production of highly chlorinated copper phthalocyanine
JPS51136632A (en) Process for preparation of dibenzamides
JPS56169650A (en) Preparation of 3-nitro-4-hydroxyphenylacetic ester
JPS55111468A (en) Preparation of n-benzyl-tetrahydro isoquinoline derivative
JPS57145860A (en) 2-halomethyl-6-phenoxypyridine derivative and its preparation
JPS5645972A (en) Release agent
JPS5547652A (en) Production of substituted sulfondiimine
JPS57134487A (en) Preparation of 7alpha-methoxycephalosporin compound
JPS56123964A (en) 1- n-benzyl-o- 2,6-dichloroanilino phenyl -2-methylsulfinyl- 2-methylthioethylene
JPS5620560A (en) Production of 2-halogenobenzonitrile derivative
JPS56100754A (en) Preparation of 2-halogenoacrylonitrile
JPS57197231A (en) Preparation of aliphatic organic chloride