Hydrogen Bromide → 5,6-Dichloro-2-trifluoromethylbenzimidazole
Reaction equation
Br.CNC(O[N:7]1[C:11]2[CH:12]=[C:13]([Cl:17])[C:14]([Cl:16])=[CH:15][C:10]=2[N:9]=[C:8]1[C:18]([F:21])([F:20])[F:19])=O>CO>[Cl:17][C:13]1[C:14]([Cl:16])=[CH:15][C:10]2[N:9]=[C:8]([C:18]([F:21])([F:19])[F:20])[NH:7][C:11]=2[CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
HBr was passed into a cooled (0° -5° C.) solution of 1.05 grams of 1-(methylcarbamoyloxy)-5,6-dichloro-2 -(trifluoromethyl) benzimidazole in 40 milliliters of methanol. The reaction mixture was permitted to stand for twenty minutes, then evaporated to obtain as a residue 5,6-dichloro-2-(trifluoromethyl) benzimidazole. After recrystallization from chloroform, it melted at 233° -5° C.
Workup
- waitto stand for twenty minutes
- customevaporated
Sources & evidence
- ORD record
- ord-eeb65c7767474d69a2639dbd568ffe22
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04031107
Reaction notes
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