1-Benzothiophene-6-carboxylic acid → 2-Boronobenzo[b]thiophene-6-carboxylic acid
Reaction equation
C([C:4]1[C:12]2[CH:11]=[C:10]([B:13]([OH:15])[OH:14])[S:9][C:8]=2[CH:7]=[CH:6][CH:5]=1)(O)=O.S1C=CC2C=CC([C:25]([OH:27])=[O:26])=CC1=2>>[C:25]([C:6]1[CH:5]=[CH:4][C:12]2[CH:11]=[C:10]([B:13]([OH:14])[OH:15])[S:9][C:8]=2[CH:7]=1)([OH:27])=[O:26]Participants
3
Procedure
The title compound (120 g, 86%) is prepared essentially as described in the preparation of 4-carboxy-benzo[b]thiophen-2-boronic acid utilizing benzo[b]thiophene-6-carboxylic acid, ES/MS m/e 221 M−1).
Sources & evidence
- ORD record
- ord-e76d52a59dbd4eb1b973a8cea3fffa20
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07863302B2
Reaction notes
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