Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetamide → 2,6-Xylyl isothiocyanate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetamide | HCID 178 | — |
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | N,N-Dimethylacetamide--benzene (1/1) | HCID 21705219 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | toluene N,N-dimethylacetamide | HCID 66603805 | — |
| 생성물 | 2,6-Xylyl isothiocyanate | HCID 87976 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04614798 |
| 출처 데이터셋 | uspto-grants-1986_09 |
| ORD ID | ord-69321b9344924861a5eab92e23c20ff5 |
| 출처 메모 | uspto-grants-1986_09 |