Phenylboronic Acid → HCID 69450238, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6](Br)=[C:5]([O:10][CH3:11])[C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18].[C:19]1(B(O)O)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[C:5]([O:10][CH3:11])[C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18]Participants
3
Procedure
This compound was prepared by the same procedure as used in EXAMPLE 3 using 1,3-dimethoxy-2-(tol-2-yl)-4-bromobenzene 2 and phenyl boronic acid to yield 34.
Workup
- customThis compound was prepared by the same procedure
Sources & evidence
- ORD record
- ord-6954e7918f134df0bd00495b2b2ab39d
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06221604B1
Reaction notes
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