돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35550생성일: 2026년 10월 24일

Hydrochloric Acid → alpha-(4-Chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile

https://huagongshe.com/ko/reaction/35550

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물2-Chloro-5-nitroanisoleHCID 70519—
반응물4-Chlorobenzyl cyanideHCID 241582—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매TetrahydrofuranHCID 8028—
생성물alpha-(4-Chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrileHCID 23035215—

반응 단계

To a stirred mixture of 68 parts of 1-chloro-2-methoxy-4-nitrobenzene, 230 parts of a sodium hydroxide solution 50%, 5 parts of N,N,N-triethylbenzenemethanaminium chloride and 360 parts of tetrahydrofuran is added dropwise, during a 5 minutes period, a solution of 43.2 parts of 4-chlorobenzeneacetonitrile in 90 parts of tetrahydrofuran. Upon completion, stirring is continued for 4 hours at 60° C. The reaction mixture is poured into 2000 parts of crushed ice. The whole is acidified with concentrated hydrochloric acid. The layers are separated. The aqueous phase is extracted with dichloromethane. The combined extracts are dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding α-(4-chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04767760
출처 데이터셋uspto-grants-1988_08
ORD IDord-fff9ae469d1a457387a4a6f72779f1b8
출처 메모uspto-grants-1988_08