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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723336Generated: October 30, 2026

Dichloromethane → 1-[4-(2-Bromoethoxy)phenyl]-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-one

https://huagongshe.com/reaction/723336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,2-DibromoethaneHCID 7839—
ReactantSodium HydroxideHCID 14798—
Reactant1-(4-Hydroxyphenyl)-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-oneHCID 21873410—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
Product1-[4-(2-Bromoethoxy)phenyl]-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-oneHCID 12095858—

Reaction Conditions

Temperature75 °C

Reaction Steps

A solution of 1-(4-hydroxyphenyl)-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-one (4.7 g) in 1,2-dibromoethane (23.6 ml) was mixed with sodium hydroxide solution (3N, 9.1 ml) and tetrabutylammonium hydrogen sulfate (232 mg). The mixture was heated at 75° C. for 2 hours. After cooling, the reaction mixture was mixed with dichloromethane and washed with sodium hydroxide solution (1N), hydrochloric acid (1N) and saturated brine. The organic phase was dried over magnesium sulfate and concentrated, and the residue was purified by chromatography on silica gel (eluent: dichloromethane/methanol 9:1). The product with the molecular weight of 451.32 (C23H19BrN2O3); MS (ESI): 451 ([M+H]+), was obtained in this way.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141561B2
Source datasetuspto-grants-2006_11
ORD IDord-fe892cbda3e64447a214492c064e3981
Source noteuspto-grants-2006_11