돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274122생성일: 2026년 10월 26일

Benzyl Chloride → 1-(Phenylmethyl)cycloheptanecarbonitrile

https://huagongshe.com/reaction/274122

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물DiisopropylamineHCID 7912—
반응물CycloheptanecarbonitrileHCID 96653—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-(Phenylmethyl)cycloheptanecarbonitrileHCID 1899962455.8%

반응 단계

Obtained by operating as in example 27b, from 195 mmoles of lithiated diisopropylamine (25.6 g (252.9 mmoles) of diisopropylamine treated with 122 ml (195 mmoles) of n-butyllithium 1.6M in hexane) in 300 ml of dry tetrahydrofuran, 24 g (195 mmoles) of commercial cycloheptanecarbonitrile and 24.6 g (195 mmoles) of benzyl chloride. After distillation, there is obtained 23.2 g (yield=55.8%) of a yellow viscous liquid. b.p.16 =190°-7° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387709
출처 데이터셋uspto-grants-1995_02
ORD IDord-8e8197743c254561b3d8266272a7e85b
출처 메모uspto-grants-1995_02