反応式
[O:1]=[CH:2][C@@H:3]([C@@H:5]([C@@H:7]([CH2:9][OH:10])[OH:8])[OH:6])[OH:4].S(=O)(=O)(O)O.[C:16](=O)([O-])[O-].[Na+].[Na+]>CO>[O:1]([CH3:16])[C@@H:2]1[O:8][C@H:7]([CH2:9][OH:10])[C@@H:5]([OH:6])[C@H:3]1[OH:4]参加物
5
反応条件
- 温度
- 0 °C
実験手順
5 g of D-Ribose was dissolved in 100 mL of methanol and cooled to 0° C. 0.5 mL of concentrated sulfuric acid was added and the solution was stored at −20° C. for 48 hrs. Solution was neutralized by passage through a bed of sodium carbonate and evaporated under vacuum to a viscous oil. Crude material was purified on a silica column eluting with 10% methanol in ethyl acetate to yield 2.1 grams of methyl β-D-ribofuranoside.
後処理
- customevaporated under vacuum to a viscous oil
- customCrude material was purified on a silica column
- washeluting with 10% methanol in ethyl acetate
出典と根拠
- ORDレコード
- ord-e17f9e9b96af4cb7b9fdfdc590781046
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08115026B2
関連ノート
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