Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethylformamide → N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Phenyl Isothiocyanate | HCID 7673 | — |
| 반응물 | 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-one | HCID 14869554 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide | HCID 135720099 | 47.9% |
반응 단계
To a mixture of 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-one, 0.37 g of phenyl isothio-cyanate, and 5 ml of dried N,N-dimethylformamide was added 0.31 g of potassium t-butoxide with under ice-cooling, followed by stirring for 5 hours under ice-cooling. Ice-water was added thereto, and the mixture was made acidic with acetic acid and extracted with diethyl ether. The extract was washed with water and dried over sodium sulfate, and the ether layer was removed by distillation. The residue was purified by silica gel column chromatography (developing solution: CH2Cl2) to obtain 0.4 g of N-phenyl-6- cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide represented by formula shown below.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05412117 |
| 출처 데이터셋 | uspto-grants-1995_05 |
| ORD ID | ord-5b12e05a7622475082ec0de4fcdad81a |
| 출처 메모 | uspto-grants-1995_05 |