HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamide → 2,6-Xylyl isothiocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamide | HCID 178 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N,N-dimethylacetamide benzene | HCID 21705219 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | toluene N,N-dimethylacetamide | HCID 66603805 | — |
| Product | 2,6-Xylyl isothiocyanate | HCID 87976 | — |
Reaction Steps
Briefly, this preparation involves first adding the acetamide to a suspension of sodium hydride in an organic solvent, preferably a N,N-dimethylacetamide/benzene solvent system. The cessation of hydrogen indicates completion of the reaction after which the reaction mixture is cooled and carbon disulfide added slowly. When tetrahydrofuran is the solvent employed, a reaction time of approximately 1.5 hours is required to provide yields in excess of 80 percent while when a mixture of N,N-dimethylacetamide/toluene is used, yields in excess of 80 percent are obtained in approximately 20 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04614798 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-69321b9344924861a5eab92e23c20ff5 |
| Source note | uspto-grants-1986_09 |