HCID 58062905, compound → HCID 66682167, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:24])[C:4]1[C:9]([O:10][CH3:11])=[CH:8][C:7]([C:12]([F:15])([F:14])[F:13])=[CH:6][C:5]=1[O:16]CC1C=CC=CC=1>C(O)C.[Pd]>[CH3:1][O:2][C:3](=[O:24])[C:4]1[C:9]([O:10][CH3:11])=[CH:8][C:7]([C:12]([F:13])([F:15])[F:14])=[CH:6][C:5]=1[OH:16]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 60 mg (0.176 mmol) 2-benzyloxy-6-methoxy-4-trifluoromethyl-benzoic acid methyl ester in 1 ml ethanol under nitrogen at room temperature, was added 8 mg (0.0071 mmol) Pd/C 10%. The mixture was stirred at room temperature under an hydrogen atmosphere for 4 hours. The catalyst was filtered, washed with dichloromethane and the filtrate was concentrated in vacuo to provide 38 mg (y: 86.1%) of the title compound as a white solid. MS (m/e): 249.0 (M−H).
Workup
- filtrationThe catalyst was filtered
- washwashed with dichloromethane
- concentrationthe filtrate was concentrated in vacuo
Sources & evidence
- ORD record
- ord-eba1f3c71fa246099085df199274a2f0
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08080541B2
Reaction notes
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