3-Bromopyridine → 5-Phenyl-2-Thiophenecarboxylic Acid
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][C:7](B(O)O)=[CH:6][CH:5]=1)(O)=O.BrC1[S:18][C:17]([C:19]([OH:21])=[O:20])=[CH:16][CH:15]=1.BrC1C=NC=CC=1>>[C:4]1([C:1]2[S:18][C:17]([C:19]([OH:21])=[O:20])=[CH:16][CH:15]=2)[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
4
Procedure
Following the procedure of Preparation 1(a), except substituting phenylboronic acid for 4-carboxybenzeneboronic acid and 5-bromo-2-thiophenecarboxylic acid for 3-bromopyridine, afforded the title compound.
Sources & evidence
- ORD record
- ord-fc264f8ce9a64d42841c9616870a57c7
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06399656B1
Reaction notes
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