Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Salicylamide → 2,2-dimethyl-3,4-dihydro-2H-1,3-benzoxazin-4-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Salicylamide | HCID 5147 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 용매 | 2,2-Dimethoxypropane | HCID 6495 | — |
| 생성물 | 2,2-dimethyl-3,4-dihydro-2H-1,3-benzoxazin-4-one | HCID 717428 | — |
반응 단계
6.86 g (50 mmol) of salicylamide was suspended in 100 ml of acetone dimethylacetal. After the addition of 2.85 g (15 mmol) of p-toluenesulfonic acid, the mixture was heated to reflux for two hours. The resulting reaction mixture was evaporated under reduced pressure. After the addition of ethyl acetate, the solvent was washed twice with a saturated aqueous solution of sodium hydrogen carbonate and once with brine. The ethyl acetate layer was dried over anhydrous sodium sulfate and the solvent was removed by evaporation under reduced pressure, to obtain 8.94 g (quantitative) of the title compound as light yellow needle-like crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05710152 |
| 출처 데이터셋 | uspto-grants-1998_01 |
| ORD ID | ord-c2af07350a1146e78187960312e477d6 |
| 출처 메모 | uspto-grants-1998_01 |