Potassium Hydroxide → (2S)-2-(2,4-Difluorophenyl)-2-oxiranemethanol

HRID 2256468Notes

Reaction equation

HRID 2256468 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C@@:9]([OH:21])([CH2:15][O:16]S(C)(=O)=O)[CH2:10]OC(=O)C.[OH-].[K+]>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C@:9]1([O:21][CH2:10]1)[CH2:15][OH:16]

Participants

4

Procedure

In 250 ml of toluene was dissolved 50 g of (S)-2-(2,4-difluorophenyl)-1-acetoxy-3-methanesulfonyloxy-2-propanol and thereto was added 250 ml of 20% aqueous solution of potassium hydroxide and then the resulting liquid was stirred at room temperature for 12 hours. A toluene-layer was separated and the aqueous layer was extracted three times with 100 mg of ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate and the solvent was removed. The residue was purified by column chromatography on silica gel to give 21 g of (S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-propanol. The optical purity thereof was determined by HPLC analysis (column: CHIRALPAK AS made by Daicel Chemical Industries, Ltd., eluent: n-hexane/isopropanol=98/2, detection wavelength: 254 nm, flow rate: 1.2 ml/min).

Workup

  1. customA toluene-layer was separated
  2. extractionthe aqueous layer was extracted three times with 100 mg of ethyl acetate
  3. dry with materialdried over anhydrous sodium sulfate
  4. customthe solvent was removed
  5. customThe residue was purified by column chromatography on silica gel

Sources & evidence

ORD record
ord-f88c8539ff7d4cc2a5a4710d44daca3a
Source dataset
uspto-grants-1997_08
Patent number
US05654472

Reaction notes

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