4,6-Dibromo-2-methylpyridin-3-ol → 6-Bromo-2-methylpyridin-3-ol
반응식
Br[C:2]1[CH:7]=[C:6]([Br:8])[N:5]=[C:4]([CH3:9])[C:3]=1[OH:10].[Li]CCCC>C1COCC1>[Br:8][C:6]1[N:5]=[C:4]([CH3:9])[C:3]([OH:10])=[CH:2][CH:7]=1참가 물질
4
반응 조건
- 온도
- -78 °C
실험 절차
4,6-Dibromo-2-methylpyridin-3-ol (15.8 g, 59.4 mmol) was dissolved in THF (200 mL). The solution was cooled to −78° C. and n-BuLi (50 mL, 125 mmol, 2.5 M in hexane) was added dropwise keeping the temperature below −78° C. The reaction mixture was allowed to stir at that temperature for 2 hours. The reaction mixture was quenched with water (50 mL) and was neutralized with 2 N HCl. The aqueous mixture was extracted with dichloromethane (2 times). The combined organic layers were dried (Na2SO4) and concentrated in vacuo to give 6-bromo-2-methylpyridin-3-ol (10.5 g, 95%) as a yellow oil. 1H-NMR (300 MHz, DMSO) 2.29 (s, 3H), 7.08 (d, 1H), 7.26 (d, 1H), 10.08 (s, 1H).
후처리
- customthe temperature below −78° C
- customThe reaction mixture was quenched with water (50 mL)
- extractionThe aqueous mixture was extracted with dichloromethane (2 times)
- dry with materialThe combined organic layers were dried (Na2SO4)
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-080edc0dc4b54d9092e0f1bddde5b292
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08828996B2
반응 노트
불러오는 중…