反応式
C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.[C:18]([O:24][CH3:25])(=[O:23])[C@@H:19]([CH2:21][OH:22])[OH:20]>COC(OC)(C)C>[CH2-:18][C:19]([CH3:21])=[O:20].[C:18]([O:24][CH3:25])(=[O:23])[C@@H:19]([CH2:21][OH:22])[OH:20]参加物
4
実験手順
Pyridinium p-toluenesulfonate (50 mg) was added to a solution of 8.3 g of (R)-methyl glycerate in 30 ml of 2,2-dimethoxypropane and the mixture was refluxed for 30 minutes. The reaction mixture was purified by columnchromatography using silica gel (120 g) and hexane:ethyl acetate (5:1) as an eluant to give 9.87 g (89%) of (R)-methyl glycerate acetonide.
後処理
- temperaturethe mixture was refluxed for 30 minutes
- customThe reaction mixture was purified by columnchromatography
出典と根拠
- ORDレコード
- ord-be803e2e7a2542ef86a45fe266a84ce0
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04344888
関連ノート
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