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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374263생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물AcrylonitrileHCID 7855—
반응물Trifluoromethyl toluidineHCID 2735932—
반응물Sodium NitriteHCID 23668193—
촉매Copper oxideHCID 14829—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-Chloro-3-(2-methyl-3-trifluoromethylphenyl)-propionitrileHCID 1980964290.1%

반응 조건

온도20 °C

반응 단계

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%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05166395
출처 데이터셋uspto-grants-1992_11
ORD IDord-4c9fd72cd36149eb9b0bb8a9aec43639
출처 메모uspto-grants-1992_11