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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928778Generated: October 26, 2026

5-Bromo-1-methyl-1H-imidazole → Bis(1-methyl-1H-imidazol-5-yl)methanone

https://huagongshe.com/reaction/928778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-methyl-1H-imidazoleHCID 1515258—
ReactantN-methoxy-N,1-dimethyl-1H-imidazole-5-carboxamideHCID 59677368—
ReactantHCID 178418443HCID 178418443—
SolventDichloromethaneHCID 6344—
ProductBis(1-methyl-1H-imidazol-5-yl)methanoneHCID 22048478—

Reaction Steps

To a solution of 5-bromo-1-methyl-1H-imidazole (1.2 g, 7.448 mmol) in DCM (10 mL) was added ethyl magnesium bromide (2.5 mL, 7.448 mmol; 3.0 M in diethyl ether) dropwise over a 10 minute period. The resulting pale yellow solution was stirred at room temperature for 15 minutes, cooled in an ice bath to 0° C. and N-methoxy-N,1-dimethyl-1H-imidazole-5-carboxamide (1.0 g, 6.206 mmol, Intermediate 39: step a) dissolved in DCM (3 mL) was added dropwise. The cold bath was removed and the reaction mixture stirred at room temperature for 48 hours. To the resulting yellow suspension was added water followed by 6 M aqueous HCl to a neutral pH (pH=6-7). The aqueous mixture was extracted with DCM (2×). The combined DCM extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The product was precipitated with Et2O, filtered and dried to provide the title compound as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290476B2
Source datasetuspto-grants-2016_03
ORD IDord-0a7063f68df6417691ce06dca780e2f2
Source noteuspto-grants-2016_03