1-(4-Nitrophenyl)-2-dimethylamino-1,3-propanediol → (S)-2-(4-difluoromethoxyphenyl)-3-methylbutyric acid
Reaction equation
[F:1][CH:2]([F:17])[O:3][C:4]1[CH:9]=[CH:8][C:7]([CH:10]([CH:14]([CH3:16])[CH3:15])[C:11]([OH:13])=[O:12])=[CH:6][CH:5]=1.[N+](C1C=CC(C(O)C(N(C)C)CO)=CC=1)([O-])=O>C1(C)C=CC=CC=1>[F:1][CH:2]([F:17])[O:3][C:4]1[CH:5]=[CH:6][C:7]([C@H:10]([CH:14]([CH3:15])[CH3:16])[C:11]([OH:13])=[O:12])=[CH:8][CH:9]=1Participants
4
Procedure
Dissolve 50 g of 2-(4-difluoromethoxyphenyl)-3-methylbutyric acid in 130 g of toluene and to this solution is added 0.24 mole of resolving agent 1-(4-nitrophenyl)-2-dimethylamino-1,3-propanediol. Heat the solution with stirring under reflux for 6 hours, then cool, filter, and transfer the resulting solids to 48.7 g of 15% hydrochloric acid. Heat the mixture with stirring at 40° C. for 2 hours and then allow the mixture to cool to room temperature. The resulting mixture is extracted with benzene 2-3 times, and the solvent benzene is then removed by distillation to give 21.75 g (yield: 43.5%) of (S)-2-(4-difluoromethoxyphenyl)-3-methylbutyric acid.
Workup
- additionto this solution is added 0.24 mole
- temperatureHeat the solution
- temperatureunder reflux for 6 hours
- temperaturecool
- filtrationfilter
- temperatureHeat the mixture
- stirringwith stirring at 40° C. for 2 hours
- extractionThe resulting mixture is extracted with benzene 2-3 times
- customthe solvent benzene is then removed by distillation
Sources & evidence
- ORD record
- ord-9504f1fd34b842b0b00ca9156d287e4a
- Source dataset
- uspto-grants-1999_03
- Patent number
- US05886207
Reaction notes
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