Furan-2-boronic acid → 2-(4-(Difluoromethoxy)-3,5-dimethoxyphenyl)furan
Reaction equation
Br[C:2]1[CH:3]=[C:4]([O:14][CH3:15])[C:5]([O:10][CH:11]([F:13])[F:12])=[C:6]([O:8][CH3:9])[CH:7]=1.[O:16]1[CH:20]=[CH:19][CH:18]=[C:17]1B(O)O>>[F:12][CH:11]([F:13])[O:10][C:5]1[C:4]([O:14][CH3:15])=[CH:3][C:2]([C:17]2[O:16][CH:20]=[CH:19][CH:18]=2)=[CH:7][C:6]=1[O:8][CH3:9]Participants
3
Procedure
5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene was coupled with 2-furylboronic acid following the procedure for the synthesis of Example 21. Purification by chromatography (0-30% EtOAc-hexanes) provided 2-(4-(difluoromethoxy)-3,5-dimethoxyphenyl)furan as a white crystalline material (0.555 g, 67% yield).
Workup
- customfor the synthesis of Example 21
- customPurification by chromatography (0-30% EtOAc-hexanes)
Sources & evidence
- ORD record
- ord-658b142ae1714a849ab0f4d9cedf4a35
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09434707B2
Reaction notes
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