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HRID 370658作成日:2026年10月26日

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

https://huagongshe.com/reaction/370658

反応式

関与物質

役割名称HCID仕込み量
反応物AnisoleHCID 7519—
反応物1-(4-Benzyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanoneHCID 10322760—
溶媒Acetic AcidHCID 176—
溶媒Hydrogen BromideHCID 260—
生成物2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanoneHCID 1034012962%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04528194
出典データセットuspto-grants-1985_07
ORD IDord-ff844af5aea943b1b43f1a93ac133f60
出典メモuspto-grants-1985_07