Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 4-Methyl-5-phenyl-2-p-tolyloxazole 3-oxide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 4-Methylbenzaldehyde | HCID 7725 | — |
| 반응물 | 1,2-Propanedione, 1-phenyl-, 2-oxime | HCID 6399024 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 4-Methyl-5-phenyl-2-p-tolyloxazole 3-oxide | HCID 58934191 | — |
반응 단계
12.5 g of 1-phenyl-1,2-propanedione-2-oxime and 10 ml of p-tolualdehyde are added to 50 ml of glacial acetic acid, and HCl gas is introduced for 30 minutes, with ice-cooling. The product is precipitated as the hydrochloride by addition of methyl tert-butyl ether and filtered off with suction, and the precipitate is washed with methyl tert-butyl ether. The precipitate is suspended in water and the pH is made alkaline using ammonia. The mixture is extracted three times with in each case 200 ml of dichloromethane, the combined organic phases are dried over MgSO4 and the solvent is then removed under reduced pressure. This gives 6.4 g of 4-methyl-5-phenyl-2-p-tolyloxazole 3-oxide as a white solid. C17H15NO2 (265.31), MS(ESI)=266 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07365084B2 |
| 출처 데이터셋 | uspto-grants-2008_04 |
| ORD ID | ord-c6d8bd31b53646a082a941b63e8f693b |
| 출처 메모 | uspto-grants-2008_04 |