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HRID 434406作成日:2026年10月27日
Ammonium Chloride → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-hydroxy-4-(4-methoxyphenyl)piperidine hydrochloride
https://huagongshe.com/reaction/434406
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-piperidone | HCID 13207819 | — |
| 反応物 | HCID 178418276 | HCID 178418276 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-hydroxy-4-(4-methoxyphenyl)piperidine hydrochloride | HCID 13207827 | — |
反応手順
A solution of 6.3 g of 1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-piperidone in 35 ml of tetrahydrofuran was slowly added to a solution of 49 ml of p-anisylmagnesium bromide (1.4 M in tetrahydrofuran). After the addition was complete, the reaction mixture was stirred at ambient temperature for one hr, diluted with ether, poured into 400 of ml saturated ammonium chloride solution and extracted with ether. The organic extracts were washed with water (2×), saturated sodium chloride solution and dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was converted to 8.5 g (89%) of product, mp 100°-105° C., by treatment with ethereal hydrogen chloride. An analytical sample was obtained by recrystallization from ethyl acetate/methanol and had mp 181°-182° C. (dec).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04396770 |
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| 出典データセット | uspto-grants-1983_08 |
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| ORD ID | ord-c19ce0116b8849bba4849a32a844be42 |
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| 出典メモ | uspto-grants-1983_08 |
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