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Hydrogen Bromide → 4-[4-(4-Aminophenyl)piperazin-1-yl]phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)- | HCID 154406 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-[4-(4-Aminophenyl)piperazin-1-yl]phenol | HCID 10221065 | 44% |
反応手順
A mixture of 30 parts of 4-[4-(4-methoxyphenyl)-1-piperazinyl]benzenamine and 300 parts of a hydrobromic acid solution 48% in water is stirred and refluxed for 10 days. The reaction mixture is evaporated and the residue is alkalized with sodium hydroxide. The mixture is filtered and the filtrate is acidified with acetic acid. The precipitated product is filtered off and crystallized from 1,4-dioxane, yielding 12 parts (44%) of 4-[4-(4-aminophenyl)-1-piperazinyl]phenol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04490530 |
| 出典データセット | uspto-grants-1984_12 |
| ORD ID | ord-476e78f0e2374da3afda6f1c0fbd12bb |
| 出典メモ | uspto-grants-1984_12 |