戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 614429作成日:2026年10月26日

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

https://huagongshe.com/reaction/614429

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Potassium CarbonateHCID 11430—
反応物p-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
溶媒1,4-DioxaneHCID 31275—
生成物1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanoneHCID 712441—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04144346
出典データセットuspto-grants-1979_03
ORD IDord-056bb84148764c28ad88c8ee0dbb26cc
出典メモuspto-grants-1979_03