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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480019Generated: November 1, 2026

Ethyl Acetate → 4-Bromo-2-ethoxy-5-methyl-1-[3-(trifluoromethyl)phenyl]-1H-imidazole

https://huagongshe.com/reaction/1480019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Ethoxy-5-methyl-1-[3-(trifluoromethyl)phenyl]-1H-imidazoleHCID 121393738—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
Product4-Bromo-2-ethoxy-5-methyl-1-[3-(trifluoromethyl)phenyl]-1H-imidazoleHCID 121393733—

Reaction Steps

A solution of NBS (5.16 g, 29 mmol) in MeCN (60 mL) was added to a stirred solution of 2-ethoxy-5-methyl-1-[3-(trifluoromethyl)phenyl]-1H-imidazole (7.92 g, 29 mmol) in MeCN (115 mL) at such a rate that the internal temperature of the mixture did not exceed 25° C. (a RT cooling bath was used). After 0.5 h the mixture was diluted with water (50 mL) and saturated sodium carbonate (aq) (50 mL). Ethyl acetate (50 mL) was added. The mixture was stirred vigorously then the phases were separated. The organic phase was washed with saturated brine (50 mL), dried (sodium sulfate) and concentrated in vacuo. The residue was taken into dichloromethane and filtered through a 25 g Si II SPE cartridge. The cartridge was washed with DCM and 10% EtOAc in DCM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409870B2
Source datasetuspto-grants-2016_08
ORD IDord-796635d23b6b48c1b8e38629ab136a81
Source noteuspto-grants-2016_08