4-Methoxycarbonylphenylboronic acid → HCID 70938355, compound
Reaction equation
[OH:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][C@@H:6]2[OH:11].[CH3:12][O:13][C:14]([C:16]1[CH:21]=[CH:20][C:19](B(O)O)=[CH:18][CH:17]=1)=[O:15]>>[OH:11][C@@H:6]1[C:7]2[C:3](=[C:2]([O:1][C:19]3[CH:20]=[CH:21][C:16]([C:14]([O:13][CH3:12])=[O:15])=[CH:17][CH:18]=3)[CH:10]=[CH:9][CH:8]=2)[CH2:4][CH2:5]1Participants
3
Procedure
According to the method of (Example 99) <Step 1>, from (1S)-4-hydroxy-2,3-dihydro-1H-inden-1-ol (0.99 g) and (4-(methoxycarbonyl)phenyl)boronic acid (1.31 g) that are commercially available or are obtained according to a known method, the subject compound (0.80 g) was obtained as pale yellow solid.
Workup
- customare obtained
Sources & evidence
- ORD record
- ord-e2c40e49838f4e9ea4c01382f0985019
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765752B2
Reaction notes
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