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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 485219생성일: 2026년 10월 25일

Hydrochloric Acid → 2-Chloro-3-phenyl-propionitrile

https://huagongshe.com/reaction/485219

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물AnilineHCID 6115—
반응물AcrylonitrileHCID 7855—
반응물Benzenamine hydrochloride (1:1)HCID 8870—
반응물Sodium NitriteHCID 23668193—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물2-Chloro-3-phenyl-propionitrileHCID 25527288%

반응 단계

55.8 g (0.6 mol) of aniline and 200 ml of a 25% hydrochloric acid aqueous solution were mixed to obtain a suspension of aniline hydrochloride. While cooling this solution to a temperature of from 0° to 10° C. from outside and stirring it, a solution prepared by dissolving 42.5 g (0.615 mol) of sodium nitrite in 85 ml of distilled water, was dropwise added over a period of about 4 hours. After the completion of the dropwise addition, the reaction mixture was stirred for about 1 hour at a temperature of from 0° to 10° C. To this solution, 200 ml of methanol and 95.4 g (1.8 mols) of acrylonitrile were added, and while stirring the mixture under cooling, 5 g of cuprous oxide powder was gradually added. The reaction mixture was stirred at a temperature of from 10° to 20° C. for 4 hours, and then methanol and unreacted acrylonitrile were distilled off by distillation. The residual solution was separated into an aqueous phase and an organic phase. The organic phase was subjected to distillation under reduced pressure, whereby 87 g (yield: 88%) of α-chloro-β-phenylpropionitrile was obtained. (b.p.: 105°-110° C./4 mmHg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04536342
출처 데이터셋uspto-grants-1985_08
ORD IDord-86aa23cfaf114fa2ad840a4b3e9d6610
출처 메모uspto-grants-1985_08