関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Anisole | HCID 7519 | — |
| 反応物 | 1-(4-Benzyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanone | HCID 10322760 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Hydrogen Bromide | HCID 260 | — |
| 生成物 | 2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone | HCID 10340129 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04528194 |
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| 出典データセット | uspto-grants-1985_07 |
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| ORD ID | ord-ff844af5aea943b1b43f1a93ac133f60 |
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| 出典メモ | uspto-grants-1985_07 |
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