関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 反応物 | 1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine | HCID 13076384 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine oxime | HCID 136408873 | 17.4% |
反応手順
A solution of 15.5 g of 1-acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine, 7.0 g of hydroxylamine hydrochloride, 9.5 g of ammonium acetate and 75 ml of water was heated under reflux for 20 hrs. The solution was poured into water and extracted with dichloromethane. The dichloromethane extract was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to give an oil. The oil was triturated with hot toluene. The toluene was decanted and the oil was triturated with ether to give a solid. The tolulene triturant, upon standing, yielded a solid. The solids were combined and recrystallized from acetonitrile to yield 2.8 g (17.4%) of product, mp, 191°-193°, as a mixture of E- and Z-isomers. The chromatogram showed 2 spots.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04528376 |
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| 出典データセット | uspto-grants-1985_07 |
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| ORD ID | ord-1b85797003b1489cb3dabf1d4a71a1a3 |
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| 出典メモ | uspto-grants-1985_07 |
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