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HRID 230982作成日:2026年10月25日

Thionyl Chloride → 4-Chloropyridine-3-carbonyl chloride

https://huagongshe.com/reaction/230982

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物4-Chloronicotinic acidHCID 818229—
生成物4-Chloropyridine-3-carbonyl chlorideHCID 13597878—

反応手順

o-Halogeno-(hetero-)aryl-carboxylic acid halides which can be employed in the process according to the invention, and processes for their preparation, are known. Thus, for example, J. Am. Chem. Soc. 40,233 (1908) describes the preparation of 2-ethylmercapto-6-chloropyrimidine-5-carboxylic acid chloride by reacting 2-ethylmercapto-4-oxo-3,4-dihydropyrimidine-5-carboxylic acid with phosphorus oxychloride. The reaction of 2-hydroxy-quinoxaline-3-carboxylic acid with thionyl chloride in the presence of a catalytic amount of dimethylformamide to give 2-chloroquinoxaline-3-carboxylic acid chloride is described in Arch. Pharm. 306, 401 (1973). The reaction 4-chloronicotinic acid with thionyl chloride under reflex to give 4-chloronicotinic acid chloride is described in J. Chem. Soc. (C), 1966, 1816.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE032975
出典データセットuspto-grants-1989_07
ORD IDord-2eb2539175204f239a80088a0e41a7a3
出典メモuspto-grants-1989_07