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

HRID 356805

반응식

HRID 356805 반응식
[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]

참가 물질

5

실험 절차

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 reactiom 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.

후처리

  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)

출처 및 근거

ORD 기록
ord-4bbd2f00e09d4caab222fa68732a9815
출처 데이터셋
uspto-grants-1998_11
특허 번호
US05840553

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