1-Benzyl-4-(2-fluorobenzyl)piperidin-4-ol → 4-[(2-Fluorophenyl)methyl]piperidin-4-ol
Reaction equation
C([N:8]1[CH2:13][CH2:12][C:11]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[F:22])([OH:14])[CH2:10][CH2:9]1)C1C=CC=CC=1>C(OCC)(=O)C.[Pd]>[F:22][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[CH2:15][C:11]1([OH:14])[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of EXAMPLE 1A (39.0 g, 131 mmol) in ethyl acetate (500 mL) was treated with Pd/C (3.90 g), stirred under hydrogen atmosphere (60 psi) until the reaction was complete by TLC analysis, and filtered. The filtrate was concentrated to give a residue that was used without further purification. MS (ESI) m/e 210 (M+H)+.
Workup
- filtrationfiltered
- concentrationThe filtrate was concentrated
- customto give a residue that
- customwas used without further purification
Sources & evidence
- ORD record
- ord-97ab637cbf584715bd81be9ea37ab8fe
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585858B2
Reaction notes
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