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

HRID 1003765

反応式

HRID 1003765 の反応式
[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]

参加物

5

反応物 3

HCID 7918Acetic AnhydrideHCID 8857Ethyl AcetateHCID 112179522-(2,4-Difluorophenyl)-1,2,3-propanetriol

生成物 1

HCID 154634621,3-Diacetoxy-2-(2,4-difluorophenyl)-2-propanol

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-21d4e998dbbf4a1da335593bc4d26aa2
出典データセット
uspto-grants-2000_04
特許番号
US06046354

関連ノート

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