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HRID 240217作成日:2026年10月26日

Thionyl Chloride → 4-Chloro-2-(chloromethyl)pyridine

https://huagongshe.com/reaction/240217

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-Chloropyridin-2-yl)methanolHCID 2763167—
溶媒DichloromethaneHCID 6344—
生成物4-Chloro-2-(chloromethyl)pyridineHCID 13052901—

反応条件

温度60 °C

反応手順

4-Chloro-2-pyridinemethanol (1.0 g, 6.965 mmol) was dissolved in dichloromethane (25 cm3), heated to reflux and then treated slowly with a solution of thionyl chloride (1.50 cm3, d=1.631 gcm−3, 0.0206 mmol) in DCM (25 cm3). The reaction mixture was then stirred at 60° C. for 3 h, soon turning pink. After this time the DCM was evaporated off and the pale pink residue carefully neutralised with saturated sodium bicarbonate solution (40 cm3). The product was then extracted into DCM (3×30 cm3) and dried over sodium carbonate for 30 min. After filtration the product solution was then concentrated to a low volume and filtered through a short silica column (1:4 methanol/DCM as eluent), giving a pale yellow solution. This was then concentrated down to a red/brown oil, dried at 50° C., which was the desired product 4-chloro-2-chloromethylpyridine (934 mg, 83%); 1H NMR (CDCl3); δH 8.40 (d, 1H, J=5.5), 7.44 (d, 1H, J=1.5), 7.19 (dd, 1H, J=5.5, 1.5), and 4.58 (s, 2H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08647781B2
出典データセットuspto-grants-2014_02
ORD IDord-aa3df7e3bb0b4f57a46dfc238f07ecad
出典メモuspto-grants-2014_02