Methyl 4-[2-(2-benzyloxyphenyl)ethyl]-3-aminobenzoate → Methyl 4-[2-(2-benzyloxyphenyl)ethyl]-2-hydroxybenzoate
Reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1/[CH:15]=[CH:16]/[C:17]1[CH:25]=[CH:24][C:20]([C:21]([OH:23])=[O:22])=[C:19]([OH:26])[CH:18]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:27](OC1C=CC=CC=1CCC1C=CC(C(OC)=O)=CC=1N)C1C=CC=CC=1>>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:15][CH2:16][C:17]1[CH:25]=[CH:24][C:20]([C:21]([O:23][CH3:27])=[O:22])=[C:19]([OH:26])[CH:18]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Methyl 4-[2-(2-benzyloxyphenyl)ethyl]-2-hydroxybenzoate was prepared from a Z/E mixture of methyl 4-[2-(2-benzyloxyphenyl)-ethenyl]-2-hydroxybenzoate (prepared as described in Example 10) using the hydrogenation method described in Example 10 for the synthesis of methyl 4-[2-(2-benzyloxyphenyl)ethyl]-3-aminobenzoate.
Sources & evidence
- ORD record
- ord-e5a3b690096444038594472ff9153389
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05811459
Reaction notes
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