Imidazole → 1-(2-chloro-4-fluorophenyl)-2-(1H-imidazol-1-yl)ethanone hydrochloride
Reaction equation
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([F:11])=[CH:7][C:6]=1[Cl:12])=[O:4].O(CC)CC.[NH:18]1[CH:22]=[CH:21][N:20]=[CH:19]1.CN(C)C=O>O>[ClH:12].[Cl:12][C:6]1[CH:7]=[C:8]([F:11])[CH:9]=[CH:10][C:5]=1[C:3](=[O:4])[CH2:2][N:18]1[CH:22]=[CH:21][N:20]=[CH:19]1Participants
Conditions
- Temperature
- 50 °C
Procedure
To a stirred solution of 78.7 parts of 2-bromo-1-(2-chloro-4-fluorophenyl)ethanone in 140 parts of 1,1'-oxybisethane are added carefully 106.4 parts of 1H-imidazole. Upon completion, there are added 180 parts of N,N-dimethylformamide and the whole is stirred for 2 hours at 50° C. After the addition of water, the product is extracted twice with trichloromethane. The combined extracts are washed three times with water, dried, filtered and evaporated. The residue is converted into the hydrochloride salt in 4-methyl-2-pentanone, 2,2'-oxybispropane and 2-propanol. The salt is filtered off and crystallized from a mixture of ethanol and 2,2'-oxybispropane, yielding 1.5 parts of 1-(2-chloro-4-fluorophenyl)-2-(1H-imidazol-1-yl)ethanone hydrochloride; mp. 197.4° C.
Workup
- extractionthe product is extracted twice with trichloromethane
- washThe combined extracts are washed three times with water
- customdried
- filtrationfiltered
- customevaporated
- filtrationThe salt is filtered off
- customcrystallized from a mixture of ethanol and 2,2'-oxybispropane
Sources & evidence
- ORD record
- ord-ec6640a85335449abe86bcec9ec70637
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04209447
Reaction notes
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