3,5-Bis-trifluoromethylphenylboronic acid → 5-(tert-Butyl)-2-hydroxy-3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-3-carbaldehyde
反応式
C(C1C=C(C=O)C(O)=C(C2C=CC(OC(F)(F)F)=CC=2)C=1)(C)(C)C.Br[C:26]1[C:27]([OH:38])=[C:28]([CH:31]=[C:32]([C:34]([CH3:37])([CH3:36])[CH3:35])[CH:33]=1)[CH:29]=[O:30].[F:39][C:40]([F:55])([F:54])[C:41]1[CH:42]=[C:43](B(O)O)[CH:44]=[C:45]([C:47]([F:50])([F:49])[F:48])[CH:46]=1>>[C:34]([C:32]1[CH:31]=[C:28]([CH:29]=[O:30])[C:27]([OH:38])=[C:26]([C:43]2[CH:44]=[C:45]([C:47]([F:50])([F:48])[F:49])[CH:46]=[C:41]([C:40]([F:39])([F:55])[F:54])[CH:42]=2)[CH:33]=1)([CH3:37])([CH3:36])[CH3:35]参加物
4
反応物 3
生成物 1
実験手順
5-(tert-Butyl)-2-hydroxy-3′,5′-bis(trifluoromethyl)-[1,1′-biphenyl]-3-carbaldehyde was prepared as an orange oil using the procedure described in Intermediate 5 from 3-bromo-5-(tert-butyl)-2-hydroxybenzaldehyde (Intermediate 4) and 3,5-bis(trifluoromethyl)phenylboronic acid.