Acetic Anhydride → 1,3-Diacetoxy-2-(2,4-difluorophenyl)-2-propanol

HRID 2256461Notes

Reaction equation

HRID 2256461 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]([OH:14])([CH2:12][OH:13])[CH2:10][OH:11].[C:15](OC(=O)C)(=[O:17])[CH3:16].[C:22](OCC)(=[O:24])[CH3:23]>N1C=CC=CC=1>[C:15]([O:11][CH2:10][C:9]([C:3]1[CH:4]=[CH:5][C:6]([F:8])=[CH:7][C:2]=1[F:1])([OH:14])[CH2:12][O:13][C:22](=[O:24])[CH3:23])(=[O:17])[CH3:16]

Participants

5

Procedure

In 100 ml of pyridine was dissolved 10 g of 2-(2,4-difluorophenyl)-1,2,3-propanetriol. To the resulting solution was added dropwise 1.1 g of acetic anhydride at room temperature. After the dropping, the resulting liquid was stirred at room temperature for 1 hour. Then, to the reaction mixture was added 50 ml of ethyl acetate, and an organic layer was separated therefrom. After the organic layer was washed with 1N aqueous solution of hydrochloric acid and further washed with water and saturated aqueous solution with sodium chloride. Then the organic layer was dried over anhydrous sodium sulfate. The resulting organic layer was filtered and the solvent was removed under reduced pressure. Thus obtained concentrate was purified by column chromatography on silica gel (hexane: ethyl acetate=1:1) to give 12.5 g of the desired compound.

Workup

  1. customan organic layer was separated
  2. washAfter the organic layer was washed with 1N aqueous solution of hydrochloric acid
  3. washfurther washed with water and saturated aqueous solution with sodium chloride
  4. dry with materialThen the organic layer was dried over anhydrous sodium sulfate
  5. filtrationThe resulting organic layer was filtered
  6. customthe solvent was removed under reduced pressure
  7. customThus obtained
  8. concentrationconcentrate
  9. customwas purified by column chromatography on silica gel (hexane: ethyl acetate=1:1)

Sources & evidence

ORD record
ord-16374436263b405593a9fcd931b63d17
Source dataset
uspto-grants-1997_08
Patent number
US05654472

Reaction notes

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