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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536628Generated: October 27, 2026

Potassium Carbonate → 1-(5-bromothiophen-2-yl)-2-methyl-1H-imidazole

https://huagongshe.com/reaction/536628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-MethylimidazoleHCID 12749—
Reactant2,5-DibromothiopheneHCID 18453—
ReactantL-ProlineHCID 145742—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product1-(5-bromothiophen-2-yl)-2-methyl-1H-imidazoleHCID 6726053231.3%

Reaction Steps

To the solution of 2,5-dibromothiophene (20 g, 82.6 mmol) and 2-methyl-1H-imidazole (4.1 g, 50 mmol) in DMSO (100 mL) was added CuI (3.14 g, 16.5 mmol), L-proline (0.95 g, 8.3 mmol), K2CO3 (22.9 g, 0.165 mol), the resultant mixture was heated to 100° C. under N2 balloon protection overnight. The reaction mixture was filtrated and the filtrate was poured into water, extracted with EtOAc (300 mL×5). The combined organic layers were washed with brine, dried over Na2SO4, and then filtrated, the filtrate was concentrated under reduced pressure, the residue was purified by column chromatography to give desired 1-(5-bromothiophen-2-yl)-2-methyl-1H-imidazole (3.8 g, yield 31.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859611B2
Source datasetuspto-grants-2014_10
ORD IDord-dccd881a0092448d903a1bfc98099c65
Source noteuspto-grants-2014_10