반응식
[Br:1][CH:2]([CH:6]([CH3:8])[CH3:7])[C:3]([OH:5])=[O:4].[CH3:9]O>>[Br:1][CH:2]([CH:6]([CH3:8])[CH3:7])[C:3]([O:5][CH3:9])=[O:4]참가 물질
3
실험 절차
2-Bromo-3-methylbutyric acid (3.65 g, 20 mmole) was esterified in refluxing methanol containing 2 mL concentrated sulfuric acid for 22 hours. After cooling to room temperature, volatiles were evaporated and the residue was taken up in 50 mL of water and extracted with Et2O. The ether layer was washed with 5% aq. NaHCO3, water brine, and dried over Na2SO4. The desired material was obtained after filtration and removal of volatiles; homogeneous by TLC in 4/1 hexane/EtOAc.
후처리
- customvolatiles were evaporated
- extractionextracted with Et2O
- washThe ether layer was washed with 5% aq. NaHCO3, water brine
- dry with materialdried over Na2SO4
출처 및 근거
- ORD 기록
- ord-98c0c321d20e4334998dacb0a35817c2
- 출처 데이터셋
- uspto-grants-1995_05
- 특허 번호
- US05411980
연결된 노트
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