Acetone → 1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose

HRID 542916

反応式

HRID 542916 の反応式
[CH3:1][C:2]([CH3:4])=[O:3].[O:5]=[CH:6][C@@H:7]([C@H:9]([C@H:11]([C@@H:13]([CH2:15][OH:16])[OH:14])[OH:12])O)[OH:8].[Sb](Cl)(Cl)(Cl)(Cl)Cl.N1C=C[CH:26]=[CH:25][CH:24]=1>>[CH3:1][C:2]1([CH3:4])[O:12][C@H:11]2[C@H:9]([C@@H:7]([CH2:6][OH:5])[O:8][C@@H:15]3[O:16][C:25]([CH3:26])([CH3:24])[O:14][C@@H:13]32)[O:3]1

参加物

5

反応条件

温度
60 °C

実験手順

To 200 ml of acetone were added 10.0 g of D-galactose and 89.7 mg of antimony pentachloride, and the mixture was refluxed with stirring in a water bath of 60° C. for 8 hours. During this reaction, the refluxing solvent was dried with 20 g of Molecular Sieves 3A interposed between the reaction vessel and the condenser. After completion of the reaction, a small amount of pyridine was added to the reaction mixture, and the acetone was distilled off under reduced pressure. The residue was dissolved in benzene, and the solution was washed with aqueous sodium bicarbonate and water, and dried over anhydrous magnesium sulfate. The benzene was distilled off, and the resulting residue was distilled under reduced pressure to give 11.97 g (82.9%) of 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose as a fraction having a boiling point of 129°-133° C./0.2 mmHg.

後処理

  1. temperaturethe mixture was refluxed
  2. customDuring this reaction
  3. dry with materialthe refluxing solvent was dried with 20 g of Molecular Sieves 3A
  4. customAfter completion of the reaction
  5. distillationthe acetone was distilled off under reduced pressure
  6. dissolutionThe residue was dissolved in benzene
  7. washthe solution was washed with aqueous sodium bicarbonate and water
  8. dry with materialdried over anhydrous magnesium sulfate
  9. distillationThe benzene was distilled off
  10. distillationthe resulting residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-47c4bc940fa54da495d155797d5e485e
出典データセット
uspto-grants-1987_04
特許番号
US04659809

関連ノート

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