関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | HCID 13192285 | HCID 13192285 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-methanesulphonyl-hexahydro-4,5-epoxy-1H-azepine | HCID 20548908 | — |
反応手順
11.7 g (0.067 mol) of 1-methanesulphonyl-2,3,6,7-tetrahydro-1H-azepine are dissolved in 230 ml of methylene chloride and the solution is treated with 23 g (0.13 mol) of m-chloro-perbenzoic acid in portions. A white suspension soon forms and this is stirred for a further 24 hours at room temperature. The m-chlorobenzoic acid which has precipitated is filtered off and the filtrate is washed with a saturated aqueous solution of sodium carbonate, then with aqueous iron-II sulphate solution, then with 0.1 N sodium hydroxide solution and finally with water and dried over sodium sulphate. On concentrating the solution under a water pump vacuum, while crystals of 1-methanesulphonyl-hexahydro-4,5-epoxy-1H-azepine are obtained and these are isolated by filtration; melting point 133°-134°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04246269 |
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| 出典データセット | uspto-grants-1981_01 |
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| ORD ID | ord-83987eeac2794123ba04aaeca279aaca |
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| 出典メモ | uspto-grants-1981_01 |
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