3-(2-Benzyloxy-3-methoxyphenyl)-5-methylhexanoic acid → Methyl 3-(4-hydroxy-2-methoxyphenyl)-5-methylhexanoate
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:14][CH2:15][CH2:16]C)[CH2:9][C:10]([O:12][CH3:13])=[O:11])=[C:4]([O:18][CH3:19])[CH:3]=1.[CH2:20](OC1C(OC)=CC=CC=1C(CC(C)C)CC(O)=O)C1C=CC=CC=1>>[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:14][CH:15]([CH3:16])[CH3:20])[CH2:9][C:10]([O:12][CH3:13])=[O:11])=[C:4]([O:18][CH3:19])[CH:3]=1Participants
3
Procedure
Following a similar procedure to that described in Preparation 58A, but using 3-(2-benzyloxy-3-methoxyphenyl)-5-methylhexanoic acid (prepared as described in Preparation 30H), the title compound was obtained as an oily substance.
Sources & evidence
- ORD record
- ord-233e881a1d1243119857c39bea3a4733
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06040339
Reaction notes
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