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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22268생성일: 2026년 10월 24일

Acrylonitrile → 3-[(3-Bromophenyl)thio]propionitrile

https://huagongshe.com/ko/reaction/22268

반응식

참여 물질

역할이름HCID투입량
반응물AcrylonitrileHCID 7855—
반응물m-BromobenzenethiolHCID 80597—
용매Sodium HydroxideHCID 14798—
생성물3-[(3-Bromophenyl)thio]propionitrileHCID 1868674293.7%

반응 단계

3-Bromothiophenol (10 g, 52.9 mmmol) was dissolved in acrylonitrile (11.28 g, 213 mmol). Triton B (1 mL) was added, at which time the reaction mixture became exothermic and began to reflux without added heat. The mixture was allowed to cool to room temperature, poured into cold aqueous sodium hydroxide (2%; 200 mL), and extracted with diethyl ether. The organic layer was dried, filtered and evaporated to provide 12 g (93%) of 3-[(3-bromophenyl)thio]propionitrile as a tan oil; 1H NMR (CDCl3) δ7.54 (s, 1H), 7.42 (d, 1H), 7.32 (d, 1H), 7.25-7.15 (m, 2H), 3.15 (t, 2H), 2.62 (t, 2H); Mass spectrum m/z 261, 259 (M+NH4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428040
출처 데이터셋uspto-grants-1995_06
ORD IDord-e11ad11d2499429e80643360e0a1b5f0
출처 메모uspto-grants-1995_06