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Ethanol → 4-(4-(Methylsulfonyl)piperazin-1-yl)phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | p-(1-Piperazinyl)phenol dihydrobromide | HCID 2723591 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(4-(Methylsulfonyl)piperazin-1-yl)phenol | HCID 640049 | — |
反応手順
To a stirred mixture of 12.9 parts of 4-(1-piperazinyl)-phenol dihydrobromide, 40 parts of ethanol and 50 parts of water are added 12.6 parts of sodium hydrogen carbonate. Then there are added dropwise 6.4 parts of methanesulfonyl chloride at 0° C. Upon completion, stirring is continued overnight. The precipitated product is filtered off and taken up in water. The whole is alkalized with a sodium hydroxide solution and stirred for 30 minutes at room temperature. The mixture is filtered over hyflo and the filtrate is acidified with acetic acid. The precipitated product is filtered off and dried, yielding 2.8 parts of 1-(4-hydroxyphenyl)-4-(methylsulfonyl)piperazine; mp. 204.9° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04223036 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-6d78a14e4bea4668a79fff0ca30a4176 |
| 出典メモ | uspto-grants-1980_09 |