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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071969Generated: November 2, 2026

Benzene → tert-butyl 2-[4-(1H-imidazol-1-yl)phenyl]ethylcarbamate

https://huagongshe.com/reaction/1071969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantImidazoleHCID 795—
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
Reactant[2-(4-Bromo-phenyl)ethyl]-carbamic acid tert-butyl esterHCID 14221818—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
Producttert-butyl 2-[4-(1H-imidazol-1-yl)phenyl]ethylcarbamateHCID 22390721—

Reaction Conditions

Temperature120 °C

Reaction Steps

Tert-butyl 2-(4-bromophenyl)ethylcarbamate (500 mg, 1.67 mmol), imidazole (170 mg, 2.50 mmol), (CuOTf)2.PhH (84 mg, 0.17 mmol), 1,10-Phenanthroline (360 mg, 2.00 mmol), dba (39 mg, 0.17 mmol), and Cs2CO3 (650 mg, 1.99 mmol) were mixed together in a flask and o-xylene (10 mL) was added. Resulting solution was heated to 120° C. and stirred for four days. Reaction mixture was then cooled, poured into water (20 mL) and extracted with EtOAc (3×20 mL). Combined organics were washed with water (1×20 mL) and brine (2×20 mL), dried over sodium sulfate, filtered, and concentrated Crude product was purified by flash chromatography eluting with 25% Hexanes in EtOAC to pure EtOAc to give tert-butyl 2-[4-(1H-imidazol-1-yl)phenyl]ethylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908921B2
Source datasetuspto-grants-2005_06
ORD IDord-7ea792682b45492ea8ca48f40ec1893d
Source noteuspto-grants-2005_06