反応式
[CH3:1][C:2]([CH3:4])=[O:3].O=[CH:6][C@@H:7]([C@H:9]([C@@H:11]([CH2:13][OH:14])[OH:12])[OH:10])[OH:8].I.N1C=C[CH:19]=[CH:18][CH:17]=1>>[CH3:1][C:2]1([CH3:4])[O:10][C@@H:9]2[C@H:11]3[O:12][C:18]([CH3:19])([CH3:17])[O:14][C@H:13]3[O:8][C@@H:7]2[CH2:6][O:3]1参加物
反応条件
- 温度
- 60 °C
実験手順
To 200 ml of acetone were added 10.0 g of D-xylose and 175 mg of hydriodic acid (57%) and the mixture was refluxed with stirring in a water bath at 60° C. for 5 hours. During this reaction, the refluxing solvent was dried with 20 g of Molecular Sieves 3A interposed between the reaction vessel and the cooling jacket. After completion of the reaction, a small amount of pyridine was added and the acetone was distilled off under reduced pressure. The residue was dissolved in benzene and the benzene solution was washed with aqueous sodium bicarbonate and water and dried over anhydrous magnesium sulfate. The benzene was distilled off under reduced pressure and the residue was further distilled under reduced pressure, whereby 12.8 g (83.6%) of 1,2:3,5-di-O-isopropylidene-α-D-xylofuranose was obtained as a fraction boiling at 94°-97° C./3 mmHg.
後処理
- temperaturethe mixture was refluxed
- customDuring this reaction
- dry with materialthe refluxing solvent was dried with 20 g of Molecular Sieves 3A
- customAfter completion of the reaction
- distillationthe acetone was distilled off under reduced pressure
- dissolutionThe residue was dissolved in benzene
- washthe benzene solution was washed with aqueous sodium bicarbonate and water
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe benzene was distilled off under reduced pressure
- distillationthe residue was further distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-76a5f66a51094a61bd512b882d9b312c
- 出典データセット
- uspto-grants-1984_08
- 特許番号
- US04464530
関連ノート
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