Lithium Hydroxide → HCID 21876358, compound
Reaction equation
C([O:4][C:5]([CH3:17])([CH3:16])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][CH:8]=1)(=O)C.[Li+].[OH-]>CO>[CH3:17][C:5]([OH:4])([CH3:16])[CH2:6][C:7]1[CH:8]=[CH:9][C:10]([N+:13]([O-:15])=[O:14])=[CH:11][CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
To a solution of 1,1-dimethyl-2-(4-nitrophenyl)ethyl acetate (52 mmol) in MeOH (50 ml) was added 4N-LiOH (40 ml) and the mixture was stirred at 50° C. for 2 h. After the solvent was removed, this mixture was diluted with water and extracted with EtOAc (4×50 ml). The organic layer was washed with brine, dried (MgSO4) and concentrated. This crude was purified by SiO2 column chromatography developing with hexane/ethyl acetate (5/1) to give the title compound as yellow oil (3.3 g, 33%).
Workup
- customAfter the solvent was removed
- additionthis mixture was diluted with water
- extractionextracted with EtOAc (4×50 ml)
- washThe organic layer was washed with brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customThis crude was purified by SiO2 column chromatography
Sources & evidence
- ORD record
- ord-10d50b2d1a8e4074af285c00fb9b779e
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07141580B2
Reaction notes
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