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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509651Generated: November 1, 2026

N,N-Dimethylglycine → HCID 118114109, compound

https://huagongshe.com/reaction/1509651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantImidazoleHCID 795—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-dibromo-5-tert-butylbenzeneHCID 2761170—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 118114109HCID 118114109—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1,3-dibromo-5-tert-butylbenzene (2.92 g, 10.0 mmol, 1.0 eq), 1H-imidazole (0.69 g, 10.0 mmol, 1.0 eq), CuI (0.19 g, 1.0 mmol, 0.10 eq), K2CO3 (2.76 g, 20.0 mmol, 2.0 eq) and 2-(dimethylamino)acetic acid (0.21 g, 2.0 mmol, 0.20 eq) in DMSO (10 mL) was stirred at a temperature of 110° C. for four days under a nitrogen atmosphere, then cooled down to ambient temperature. The mixture was diluted with plenty of ethyl acetate and filtered. The filtrate was washed with water three times, dried over sodium sulfate, then filtered, and the filtrate was concentrated under reduced pressure. The residue was purified through column chromatography on silica gel using hexane and ethyl acetate as an eluent to obtain the desired product, 1-(3-bromo-5-tert-butylphenyl)-1H-imidazole 7, as a brown sticky liquid (1.56 g in 56% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09224963B2
Source datasetuspto-grants-2015_12
ORD IDord-26c0243dd5c143d58666e829b57b7d8e
Source noteuspto-grants-2015_12