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Triethylamine → 1-[(1-Phenylethyl)sulfanyl]pyrrolidine-2,5-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Chlorosuccinimide | HCID 31398 | — |
| 反応物 | 1-Phenylethanethiol | HCID 141850 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 1-[(1-Phenylethyl)sulfanyl]pyrrolidine-2,5-dione | HCID 20554617 | 36.8% |
反応手順
To a suitable reactor equipped with temperature controlling means and stirring means, there are charged, while maintaining the temperature at about room temperature, N-chlorosuccinimide (about 0.30 mole) in 400 ml of benzene and 1-phenylethanethiol (about 0.30 mole) in 50 ml of benzene. After stirring the reaction mixture 10 minutes, triethylamine (0.32 mole) in 50 ml of benzene is added dropwise. The benzene mixture is stirred one hour and then filtered. The filtrate is washed three times with 250 ml portions of water and then subjected to vacuum with heating to strip off volatile components. A crystalline residue is recrystallized from ethanol to give 26 grams of N-(α-methylbenzylthio)succinimide, m.p. 121-125°C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04080342 |
| 出典データセット | uspto-grants-1978_03 |
| ORD ID | ord-a910ef935e39498f9cd87e7681119e55 |
| 出典メモ | uspto-grants-1978_03 |