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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 908092생성일: 2026년 10월 24일

P-Chloroacetophenone → p-Chlorophenacyl bromide

https://huagongshe.com/ko/reaction/908092

반응식

참여 물질

역할이름HCID투입량
반응물P-ChloroacetophenoneHCID 7467—
용매Acetic AcidHCID 176—
생성물p-Chlorophenacyl bromideHCID 68303—
생성물2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochlorideHCID 2798211—

반응 단계

The starting 2-amino-1-(4-chlorophenyl)ethanone hydrochloride was prepared according to the following procedure. The 1-(4-chlorophenyl)ethanone (1.0 eq.) was dissolved in glacial acetic acid (1 ml, per mmol). To this was added a slurry of pyridinium bromide perbromide (1.03 eq.) in acetic acid (1 mL per mmol). The heterogeneous mixture was stirred for 4 h at ambient temperature. After about 30 min. the mixture turned homogeneous. After pouring into ice-water a yellow precipitate was filtered off and washed with water (2×1 mL per mmol of starting ketone). Drying of the precipitate afforded 2-bromo-1-(4-chlorophenyl)ethanone in ca. 90% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017555B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-c36b39ac91384ba699e4e403ccd48175
출처 메모uspto-grants-2011_09