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Hydrogen Sulfide → HCID 178523349、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Sulfide | HCID 402 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-(((Benzyloxy)carbonyl)amino)butanoic acid | HCID 21184 | — |
| 反応物 | Isobutyl chloroformate | HCID 62365 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 178523349 | HCID 178523349 | — |
反応手順
2.2 g (20 mmol) of triethylamine and a solution of 1.4 ml (10 mmol) of isobutyl chloroformate in 20 ml of dry methylene chloride are added dropwise, in succession, to a solution, cooled to -10°, of 2.37 g (10 mmol) of 4-benzyloxycarbonylaminobutyric acid in 50 ml of dry methylene chloride. The reaction mixture is stirred for one hour at -10° and then a strong current of hydrogen sulphide is passed through for 11/2 hours. After warming to room temperature, the mixture is cooled again and acidified with 2N sulphuric acid. The organic phase is separated, dried and concentrated in vacuo. The 4-benzyloxycarbonylaminothiobutyric acid obtained can be used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04515717 |
| 出典データセット | uspto-grants-1985_05 |
| ORD ID | ord-3f676cbf60284747a21171f1af3bf556 |
| 出典メモ | uspto-grants-1985_05 |