Dichloromethane → 1-(1,3-diisopropyldibenzo[b,d]furan-4-yl)-2-phenyl-1H-imidazole
Reaction equation
[Mn]([O-])(=O)(=O)=O.[K+].O.[O-2].[O-2].[O-2].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.[Al+3].[Al+3].ClCCl.[CH:28]([C:31]1[C:39]2[C:38]3[CH:40]=[CH:41][CH:42]=[CH:43][C:37]=3[O:36][C:35]=2[C:34]([N:44]2[CH2:48][CH2:47][N:46]=[C:45]2[C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=2)=[C:33]([CH:55]([CH3:57])[CH3:56])[CH:32]=1)([CH3:30])[CH3:29]>C(#N)C>[CH:28]([C:31]1[C:39]2[C:38]3[CH:40]=[CH:41][CH:42]=[CH:43][C:37]=3[O:36][C:35]=2[C:34]([N:44]2[CH:48]=[CH:47][N:46]=[C:45]2[C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=2)=[C:33]([CH:55]([CH3:57])[CH3:56])[CH:32]=1)([CH3:30])[CH3:29]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
The potassium permanganate (5.58 g, 35.3 mmol) and Montmorillonite K-10 clay (10 g) were mixed and finely grounded. The mixture was slowly (about 15 minutes) added into the mixed solution of dichloromethane (50 mL), acetonitrile (150 mL) and 1-(1,3-diisopropyldibenzo[b,d]furan-4-yl)-2-phenyl-4,5-dihydro-1H-imidazole (7 g, 17.6 mmol), which was cooled by ice bath. Then the reaction was stirred for another hour and quenched by adding 20 mL of ethanol. Filtered through a Celite plug. The crude product was purified by silica gel column (up to 30% EtOAc in hexanes) and recrystallization from hexane. 1-(1,3-diisopropyldibenzo[b,d]furan-4-yl)-2-phenyl-1H-imidazole (2.6 g, 6.57 mmol, 37.2% yield) was obtained as white solid (99.8% HPLC).
Workup
- custom(about 15 minutes)
- temperaturewas cooled by ice bath
- customquenched
- additionby adding 20 mL of ethanol
- filtrationFiltered through a Celite plug
- customThe crude product was purified by silica gel column (up to 30% EtOAc in hexanes) and
- customrecrystallization from hexane
Sources & evidence
- ORD record
- ord-b9cf82109cc14a8c9933ac1b97df14e6
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09156870B2
Reaction notes
Loading…