戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 374263作成日:2026年10月24日

Hydrochloric Acid → 2-Chloro-3-(2-methyl-3-trifluoromethylphenyl)-propionitrile

https://huagongshe.com/ja/reaction/374263

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物AcrylonitrileHCID 7855—
反応物Trifluoromethyl toluidineHCID 2735932—
反応物Sodium NitriteHCID 23668193—
触媒Copper oxideHCID 14829—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-Chloro-3-(2-methyl-3-trifluoromethylphenyl)-propionitrileHCID 1980964290.1%

反応条件

温度20 °C

反応手順

20 mol of concentrated hydrochloric acid is added at 0°-5° C. to a suspension of 16.7 g of 2-methyl-3-trifluoromethylaniline (0.095 mol) in 50 ml mixture is then briefly warmed to 60°-80° C. until a clear solution has formed. The solution is cooled very rapidly to 0°-5° C. with vigorous stirring, 22.4 ml (0.286 mol) of acrylonitrile are added dropwise to the fine suspension at 0°-5° C. and a solution of 6.75 g of sodium nitrite in 10 ml of water is then rapidly added, and the mixture is kept at 5° C. for a further 5 minutes and stirred at 20° C for 1 hour. After cooling, 0.8 g of copper(II) oxide powder is added to the reaction mixture at 0°-10° C. in portions, a vigorous evolution of nitrogen gas occurring. After completion of the evolution of gas, the mixture is stirred for a further 2 hours at 0°-10° C., then for 15 hours at room temperature, dichloromethane is added, and the mixture is washed with water, dried over sodium sulphate and concentrated in vacuo. 21.2 g (90% of theory) of 2-chloro-3-(2-methyl-3-trifluoromethylphenyl)-propionitrile are obtained as a brown oil. M/e 247 (M+), 228, 212, 173 (100%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05166395
出典データセットuspto-grants-1992_11
ORD IDord-4c9fd72cd36149eb9b0bb8a9aec43639
出典メモuspto-grants-1992_11