反応式
[O:1]1[CH:5]2[O:6][CH2:7][CH2:8][CH:4]2[CH:3]([OH:9])[CH2:2]1.C(N(CC)CC)C.[C:17](OC(=O)C)(=[O:19])[CH3:18]>ClCCl>[C:17]([O:9][CH:3]1[CH:4]2[CH:5]([O:6][CH2:7][CH2:8]2)[O:1][CH2:2]1)(=[O:19])[CH3:18]参加物
反応条件
- 温度
- 5 °C
実験手順
Hexahydrofuro[2,3-b]furan-3-ol (25 g) was dissolved in dichloromethane (250 ml) and added triethylamine (23.3 g). N,N-dimethylaminopyridine (0.46 g) was added to the reaction mass. Reaction mass was cooled to 0-10° C. Acetic anhydride (21.5 g) was diluted with dichloromethane (50 ml) & added slowly drop-wise to the reaction mass. Reaction mass was stirred at 0-5° C. till completion. Reaction mass was washed with water (2×100 ml) & 10% Sodium chloride solution (100 ml). Reaction mass was concentrated under vacuum at <40° C. to get residue of Hexahydrofuro[2,3-b]furan-3-yl acetate (yield 29 g). Further, the product was purified by distillation (20 g) under vacuum using fractional distillation at 88-102° C. to get main fraction 17 g having purity 92.6%
後処理
- customReaction mass
- additionadded slowly
- customReaction mass
- customReaction mass
- washwas washed with water (2×100 ml) & 10% Sodium chloride solution (100 ml)
- customReaction mass
- concentrationwas concentrated under vacuum at <40° C.
出典と根拠
- ORDレコード
- ord-a7dd7ca8078f4adcb4feb2a925d82b30
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841467B2
関連ノート
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