HCID 68610899, compound → HCID 46214026, compound
Reaction equation
C([O:8][C:9]1[CH:14]=[C:13]([O:15]CC2C=CC=CC=2)[CH:12]=[CH:11][C:10]=1[CH:23]1[CH2:26][N:25]([C:27]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[O:28])[CH2:24]1)C1C=CC=CC=1>CO.[Pd]>[OH:8][C:9]1[CH:14]=[C:13]([OH:15])[CH:12]=[CH:11][C:10]=1[CH:23]1[CH2:24][N:25]([C:27]([C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)=[O:28])[CH2:26]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
In a 10 ml round-bottomed flask, 0.2 g of [3-(2,4-bis(benzyloxy)phenyl)azetidin-1-yl]phenylmethanone is dissolved in 6 ml of methanol in the presence of 0.1 g of palladium-on-charcoal at 10%. The reaction mixture is stirred for 18 hours under a hydrogen atmosphere. The reaction mixture is filtered and the residue is then chromatographed on silica gel (1/1 heptane/ethyl acetate).
Workup
- filtrationThe reaction mixture is filtered
- customthe residue is then chromatographed on silica gel (1/1 heptane/ethyl acetate)
Sources & evidence
- ORD record
- ord-f8a1844f6317496da870bb9b516adad3
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08697726B2
Reaction notes
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