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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370658생성일: 2026년 10월 25일

Anisole → 2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone

https://huagongshe.com/reaction/370658

반응식

참여 물질

역할이름HCID투입량
반응물AnisoleHCID 7519—
반응물1-(4-Benzyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanoneHCID 10322760—
용매Acetic AcidHCID 176—
용매Hydrogen BromideHCID 260—
생성물2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanoneHCID 1034012962%

반응 단계

12.5 g (26 mmol) of 1-(4-benzyloxyphenyl)-2-(4-diphenylmethyl-piperazinyl)ethanone and 2.8 g (26 mmol) of anisole were dissolved in a mixture of 37.5 ml of acetic acid and 12.5 ml of 47% hydrobromic acid. The resultant mixture was heated to reflux for 1 hour. After being cooled to room temperautre, the reaction mixture was washed with 200 ml of ether and then with 50 ml of ether to remove acetic acid. The resultant solution was neutralized with an aqueous 2N solution of sodium hydroxide. Separated organic substances were extracted with 120 ml of ethyl acetate and then washed with saturated saline. The ethyl acetate solution was dried over anhydrous sodium sulfate and then concentrated. The residue was taken up in 60 ml of isopropanol and allowed to stand at room temperature to give 6.28 g of crude crystals of 2-(4-diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone (yield: 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04528194
출처 데이터셋uspto-grants-1985_07
ORD IDord-ff844af5aea943b1b43f1a93ac133f60
출처 메모uspto-grants-1985_07