참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Acetyl-5-bromopyridine | HCID 820423 | — |
| 반응물 | HCID 178418573 | HCID 178418573 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(5-Bromo-3-pyridyl)propan-2-ol | HCID 22391966 | — |
반응 단계
Methyl magnesium bromide (5.3 mL, 0.075 mol) was added to a stirred solution of 1-(5-bromopyridin-3-yl)ethanone (1.0 g, 0.05 mol) in tetrahydrofuran (20.0 mL), cooled to 0° C. and the resulting mixture was allowed to warm to room temperature and stirred for 1.5 h. The reaction mixture was quenched with 1N hydrochloric acid (20 mL) and extracted with ethyl acetate (2×75 mL). The combined organic layers were dried over sodium sulphate and concentrated under vacuum to afford the crude compound which was purified by column chromatography to obtain 2-(5-bromopyridin-3-yl)propan-2-ol. MS (M+1): 217.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09351973B2 |
|---|
| 출처 데이터셋 | uspto-grants-2016_05 |
|---|
| ORD ID | ord-78161fb62e904e78b4b4173b12300011 |
|---|
| 출처 메모 | uspto-grants-2016_05 |
|---|