反応式
[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]参加物
3
実験手順
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.
後処理
- customvolatiles were evaporated
- extractionextracted with Et2O
- washThe ether layer was washed with 5% aq. NaHCO3, water brine
- dry with materialdried over Na2SO4
出典と根拠
- ORDレコード
- ord-98c0c321d20e4334998dacb0a35817c2
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05411980
関連ノート
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