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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167315Generated: November 3, 2026

Hydrochloric Acid → Ethyl 2-cyclopentyloxy-4-methoxy-benzimidate hydrochloride

https://huagongshe.com/reaction/1167315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant2-Cyclopentyloxy-4-methoxy-benzonitrileHCID 22721165—
ProductEthyl 2-cyclopentyloxy-4-methoxy-benzimidate hydrochlorideHCID 22721083—

Reaction Steps

Hydrogen chloride gas was passed through a solution of 2-cyclopentyloxy-4-methoxy-benzonitrile (120 mg, 0.552 mmol) in anhydrous ethanol (15 mL) at 0° C. After 45 min, hydrogen chloride gas was stopped and the reaction vessel was sealed with a septum. After stirring at room temperature for 3 d, the reaction vessel was cooled to 0° C. and the septum was removed. The solvent was removed in vacuo to afford ethyl 2-cyclopentyloxy-4-methoxy-benzimidate hydrochloride as a yellow oil (169 mg). It was dissolved methanol (2 mL) and meso-1,2-bis-(4-chloro-phenyl)-ethane-1,2-diamine (160 mg, 0.569 mmol) was added. The solution was heated at 85° C. for 2 h. The solvent was removed and the residue was taken into diethyl ether. It was washed with sodium bicarbonate solution, water and dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel) eluting with 0-25% diethyl ether in methylene chloride to afford 4,5-bis-(4-chloro-phenyl)-2-(2-cyclopentyloxy-4-methoxy-phenyl)-4,5-dihydro-1H-imidazole as a white foam (102 mg, 37%). HR-MS (ES, m/z) calculated for C27H27N2O2Cl2 [(M+H)+] 481.1448, observed 481.1444.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617346B1
Source datasetuspto-grants-2003_09
ORD IDord-4e02999e87724a9982228411f9c04115
Source noteuspto-grants-2003_09