化工社化工社 化学情報印刷レポート · 研究参考用
Carbon Disulfide → 2,6-Xylyl isothiocyanate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | N-Acetyl-2,6-xylidine | HCID 16616 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | 2,6-Xylyl isothiocyanate | HCID 87976 | 74.7% |
反応手順
To a suspension of 2.5 g (0.05 mol) of sodium hydride in a mixture of 40 ml of dry-dimethylacetamide and 40 ml of dry benzene, 0.05 mole of N-(2,6-dimethylphenyl)acetamide was added. After evolution of hydrogen ceased, the mixture was cooled in ice and water, and with stirring 0.075 mole of carbon disulfide was added slowly. The mixture was stirred at room temperature for 20 minutes. The reaction mixture was poured into water and extracted with toluene. The organic layer, dried over sodium sulfate, was evaporated, and distillation of the residue yielded 6.1 g (74%) of 2,6-dimethylphenylisothiocyanate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04614798 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-82b7b712d0e94545b1bc2ab0815b792f |
| 出典メモ | uspto-grants-1986_09 |