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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27725생성일: 2026년 10월 25일

Acetic Anhydride → 1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone

https://huagongshe.com/reaction/27725

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Potassium CarbonateHCID 11430—
반응물p-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
용매1,4-DioxaneHCID 31275—
생성물1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanoneHCID 712441—

반응 단계

A mixture of 33.8 parts of 4-(1-piperazinyl)-phenol dihydrobromide, 11.2 parts of acetic acid anhydride, 42 parts of potassium carbonate and 300 parts of 1,4-dioxane is stirred and refluxed for 3 days. The reaction mixture is filtered and the filtrate is evaporated. The solid residue is stirred in water and sodium hydrogen carbonate is added. The whole is stirred for 30 minutes. The precipitated product is filtered off and dissolved in a diluted hydrochloric acid solution. The solution is extracted with trichloromethane. The acid aqueous phase is separated and neutralized with ammonium hydroxide. The product is filtered off and crystallized from ethanol, yielding 5.7 parts of 1-acetyl-4-(4-hydroxyphenyl)piperazine; mp. 181.3° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04223036
출처 데이터셋uspto-grants-1980_09
ORD IDord-d4bbafb5b66547a6989a439cfdfa20d9
출처 메모uspto-grants-1980_09