3-Benzo[1,3]dioxol-5-yl-5-benzyloxy-benzoic Acid tert-butyl Ester → 3-Benzo[1,3]dioxol-5-yl-5-hydroxy-benzoic Acid tert-butyl Ester
Reaction equation
C(OC(C1C=C(C2C=CC=C(F)C=2)C=C(O)C=1)=O)(C)(C)C.[C:22]([O:26][C:27](=[O:51])[C:28]1[CH:33]=[C:32]([O:34]CC2C=CC=CC=2)[CH:31]=[C:30]([C:42]2[CH:50]=[CH:49][C:45]3[O:46][CH2:47][O:48][C:44]=3[CH:43]=2)[CH:29]=1)([CH3:25])([CH3:24])[CH3:23]>>[C:22]([O:26][C:27](=[O:51])[C:28]1[CH:33]=[C:32]([OH:34])[CH:31]=[C:30]([C:42]2[CH:50]=[CH:49][C:45]3[O:46][CH2:47][O:48][C:44]=3[CH:43]=2)[CH:29]=1)([CH3:25])([CH3:23])[CH3:24]Participants
3
Procedure
The title compound was prepared in the same way as 3′-fluoro-5-hydroxy-biphenyl-3-carboxylic acid tert-butyl ester starting from 3-benzo[1,3]dioxol-5-yl-5-benzyloxy-benzoic acid tert-butyl ester.
Sources & evidence
- ORD record
- ord-ef36ab1282544ea1b74e091a72f95910
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989454B2
Reaction notes
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