JPS5697271A - Preparation of dihalogeno-5-trifluoromethylpyridine - Google Patents

Preparation of dihalogeno-5-trifluoromethylpyridine

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Publication number
JPS5697271A
JPS5697271A JP17276279A JP17276279A JPS5697271A JP S5697271 A JPS5697271 A JP S5697271A JP 17276279 A JP17276279 A JP 17276279A JP 17276279 A JP17276279 A JP 17276279A JP S5697271 A JPS5697271 A JP S5697271A
Authority
JP
Japan
Prior art keywords
halogeno
dihalogeno
trifluoromethylpyridine
trifluoromethyl
amino
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
JP17276279A
Other languages
Japanese (ja)
Inventor
Isao Yokomichi
Takahiro Haga
Kuniaki Hase
Toshio Nakajima
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 JP17276279A priority Critical patent/JPS5697271A/en
Publication of JPS5697271A publication Critical patent/JPS5697271A/en
Pending legal-status Critical Current

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  • Pyridine Compounds (AREA)

Abstract

PURPOSE: To obtain the titled substance in high yield, by halogenating trifluoromethyl-2-aminopyridine, reacting the halogenation product with a nitrite, and halogenating a 3-halogeno-5-trifluoromethylpyridone formed as a by-rpoduct.
CONSTITUTION: 2-Amino-5(or-3)-trifluoromethylpyridine is reacted with a halogenating agent in the presence of acetic, hydrochloric or hydrobromic acid to give a 2-amino-3-halogeno-5-trifluoromethyl(or 2-amino-3-trifluoromethyl-5-halogeno)pyridine, which is then reacted with a nitrite at -10W55°C to afford a 2,3-dihalogeno(or 3,6-dihalogeno)-5-trifluoromethylpyridine. The 3-halogeno-5-trifluoromethylpyridione formed as a by-product in the previous stage is further halogenated at 20W 150°C and converted into the aimed substance.
COPYRIGHT: (C)1981,JPO&Japio
JP17276279A 1979-12-28 1979-12-28 Preparation of dihalogeno-5-trifluoromethylpyridine Pending JPS5697271A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17276279A JPS5697271A (en) 1979-12-28 1979-12-28 Preparation of dihalogeno-5-trifluoromethylpyridine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17276279A JPS5697271A (en) 1979-12-28 1979-12-28 Preparation of dihalogeno-5-trifluoromethylpyridine

Publications (1)

Publication Number Publication Date
JPS5697271A true JPS5697271A (en) 1981-08-05

Family

ID=15947856

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17276279A Pending JPS5697271A (en) 1979-12-28 1979-12-28 Preparation of dihalogeno-5-trifluoromethylpyridine

Country Status (1)

Country Link
JP (1) JPS5697271A (en)

Cited By (2)

* 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
WO2018186460A1 (en) * 2017-04-04 2018-10-11 石原産業株式会社 Method for purifying trifluoromethylpyridine compound

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
WO2018186460A1 (en) * 2017-04-04 2018-10-11 石原産業株式会社 Method for purifying trifluoromethylpyridine compound
US10882824B2 (en) 2017-04-04 2021-01-05 Ishihara Sangyo Kaisha, Ltd. Method for purifying trifluoromethylpyridines

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