HCID 15044977, compound → HCID 15044979, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:15]([CH2:19][CH2:20][CH:21]([C:25]2[CH:30]=[C:29]([O:31][CH3:32])[C:28]([O:33][CH3:34])=[C:27]([O:35][CH3:36])[CH:26]=2)[C:22]([OH:24])=O)C(O)=O)[CH:6]=[C:7]([S:13][CH3:14])[C:8]=1[O:9][CH2:10][CH2:11][CH3:12].BrC1C=C(C2CCC(C3C=C(OC)C(OC)=C(OC)C=3)C2=O)C=C(OC)C=1OCCC>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:15]2[CH2:19][CH2:20][CH:21]([C:25]3[CH:30]=[C:29]([O:31][CH3:32])[C:28]([O:33][CH3:34])=[C:27]([O:35][CH3:36])[CH:26]=3)[C:22]2=[O:24])[CH:6]=[C:7]([S:13][CH3:14])[C:8]=1[O:9][CH2:10][CH2:11][CH3:12]Participants
3
Procedure
Following substantially the same procedure of Step I but substituting 2-(3-bromo-5-methoxy-6-propoxyphenyl)-5-(3,4,5-trimethoxyphenyl)-1,6-hexanedioic acid for 2-(3-methoxy-5-(methylthio)-4-propoxyphenyl)-5-(3,4,5-trimethoxyphenyl)-1,6-hexanedioic acid there was prepared a 1:4 cis:trans mixture of 2-(3-bromo-5-methoxy-4-propoxyphenyl-5-(3,4,5-trimethoxyphenyl)cyclopentanone as an oil in a 15% yield.
Workup
- customwas prepared a 1:4 cis
Sources & evidence
- ORD record
- ord-21e59ee199334cc1827b3cd293a83747
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05132463
Reaction notes
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