Methanol → Ethyl 6-(4-fluorophenyl)-5-hydroxy-6-oxohexanoate

HRID 395658Notes

Reaction equation

HRID 395658 reaction equation
Br[CH:2]([C:11]([C:13]1[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=1)=[O:12])[CH2:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7].C([O-])=[O:21].[Na+].CO>C(OCC)(=O)C>[F:19][C:16]1[CH:17]=[CH:18][C:13]([C:11](=[O:12])[CH:2]([OH:21])[CH2:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:14][CH:15]=1

Participants

5

Reactant 3

HCID 887MethanolHCID 2723810Sodium FormateHCID 18174689Ethyl 5-bromo-6-(4-fluorophenyl)-6-oxohexanoate

Product 1

HCID 18174685Ethyl 6-(4-fluorophenyl)-5-hydroxy-6-oxohexanoate

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

A mixture of ethyl 5-bromo-6-(4-fluorophenyl)-6-oxohexanoate (17.6 g), sodium formate (16.9 g) and methanol (150 ml) was stirred with heating under reflux for 16 hours. The reaction mixture was diluted with ethyl acetate (500 ml), and washed with water (200 ml×2). The organic layer was dried over anhydrous magnesium sulfate and then concentrated, the residue was subjected to silica gel column chromatography, and ethyl 6-(4-fluorophenyl)-5-hydroxy-6-oxohexanoate was obtained as a yellow oil (13.8 g, 96%) from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.

Workup

  1. temperaturewith heating
  2. temperatureunder reflux for 16 hours
  3. washwashed with water (200 ml×2)
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-030fcdd74de14a52a116f4fcf1d63b14
Source dataset
uspto-grants-2003_08
Patent number
US06605629B1

Reaction notes

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