HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Carbon Disulfide → 2,6-Xylyl isothiocyanate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | N-Acetyl-2,6-xylidine | HCID 16616 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 2,6-Xylyl isothiocyanate | HCID 87976 | 74,7% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04614798 |
| Quelldatensatz | uspto-grants-1986_09 |
| ORD ID | ord-82b7b712d0e94545b1bc2ab0815b792f |
| Quellennotiz | uspto-grants-1986_09 |