Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Acetylbenzofuran → 1-(2-Benzofuranyl)-1-(4-methyl-5-thiazolyl)ethanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Acetylbenzofuran | HCID 15435 | — |
| 반응물 | 4-Methyl-2-trimethylsilylthiazole | HCID 11658354 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 1-(2-Benzofuranyl)-1-(4-methyl-5-thiazolyl)ethanol | HCID 18936360 | — |
반응 단계
n-Butyllithium (2.5M solution in hexane, 1 equivalent) was added dropwise to a solution of 4-methyl-2-trimethylsilylthiazole (1 equivalent) in dry diethyl ether at -70° C. under an atmosphere of dry nitrogen. After 30 minutes, 2-acetylbenzofuran (1 equivalent) in diethyl ether was added. After 1 hour the mixture was allowed to warm to room temperature and was then quenched by the addition of saturated aqueous sodium hydrogen carbonate. Work up in the normal fashion and column chromatography on silica gel then afforded the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05607956 |
| 출처 데이터셋 | uspto-grants-1997_03 |
| ORD ID | ord-88731ae77d054933bd9f358b10a06bda |
| 출처 메모 | uspto-grants-1997_03 |