2-Bromo-5-vinylthiophene → 2-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-vinylthiophene
Reaction equation
[CH2:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[C:14]([F:16])[C:13](B(O)O)=[C:12]([F:20])[CH:11]=2)=[CH:6][CH:5]=1)[CH2:2][CH3:3].Br[C:22]1[S:23][C:24]([CH:27]=[CH2:28])=[CH:25][CH:26]=1>>[F:20][C:12]1[CH:11]=[C:10]([C:7]2[CH:8]=[CH:9][C:4]([CH2:1][CH2:2][CH3:3])=[CH:5][CH:6]=2)[CH:15]=[C:14]([F:16])[C:13]=1[C:22]1[S:23][C:24]([CH:27]=[CH2:28])=[CH:25][CH:26]=1Participants
3
Procedure
The compound 2-(3,5-difluoro-4′-propylbiphenyl-4-yl)-5-vinylthiophene (PUS-3-V) is prepared analogously to Example 3 from 4′-propyl-3,5-difluoro-4-biphenylboronic acid and 2-bromo-5-vinylthiophene.
Sources & evidence
- ORD record
- ord-2f5d5a5894e8434aa59ebabc8acdc109
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906261B2
Reaction notes
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