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

HRID 358130

Reaction equation

HRID 358130 reaction equation
[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].I.N1C=C[CH:21]=[CH:20][CH:19]=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:20]([CH3:21])([CH3:19])[O:14][C@@H:13]32)[O:3]1

Participants

5

Conditions

Temperature
60 °C

Procedure

To 200 ml of acetone were added 10.0 g of D-galactose and 175 mg of hydriodic acid (57%) and the mixture was refluxed with stirring in a water bath at 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 cooling jacket. After completion of the reaction, a small amount of pyridine was added. The acetone was then distilled off under reduced pressure and the residue was dissolved in benzene, washed with aqueous sodium bicarbonate and water and dried over anhydrous magnesium sulfate. The benzene was distilled off and the residue was further distilled under reduced pressure, whereby 8.5 g (59%) of 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose was obtained as a fraction boiling at 129°-133° C./0.2 mmHg.

Workup

  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 then distilled off under reduced pressure
  6. dissolutionthe residue was dissolved in benzene
  7. washwashed with aqueous sodium bicarbonate and water
  8. dry with materialdried over anhydrous magnesium sulfate
  9. distillationThe benzene was distilled off
  10. distillationthe residue was further distilled under reduced pressure

Sources & evidence

ORD record
ord-e31072d1455645e8abf04f83ad25f564
Source dataset
uspto-grants-1984_08
Patent number
US04464530

Linked notes

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