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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232322Generated: October 25, 2026

Water → 2-[4-(1H-imidazol-1-yl)phenoxy]-N-(phenylmethyl)ethanamine

https://huagongshe.com/reaction/232322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-(p-Hydroxyphenyl)imidazoleHCID 82315—
ReactantBenzenemethanamine, N-(2-chloroethyl)-, hydrochloride (1:1)HCID 13054189—
SolventDimethylformamideHCID 6228—
SolventDichloromethane methanolHCID 21226129—
Product2-[4-(1H-imidazol-1-yl)phenoxy]-N-(phenylmethyl)ethanamineHCID 14555625—

Reaction Steps

To a chilled suspension of 39.5 g (0.823 mol) 50% sodium hydride in 500 mL dimethylformamide add 37.32 g (0.233 mol) 4-(1H imidazol-1-yl)phenol. When the addition is complete, stir the reaction mixture at room temperature until gas evolution ceases. After this time, chill the reaction mixture below 0° C. and slowly add 60.22 g (0.292 mol) N-benzyl(2-chloro)ethylamine hydrochloride. When the addition is complete, heat the reaction mixture to 65° C. Follow the progress of the reaction by thin-layer chromatography on silica gel (methylene chloride:methanol) (9:1). At the completion of the reaction, add 20 mL water to the cooled mixture. Filter the slats and remove the solvents in vacuo to obtain an oil. Column chromatograph the oil on silica gel using methylene chloride+methanol (1+99→1+19) as eluent. Collect the appropriate fractions and remove the solvents to obtain the title compound as the free base. Dissolve the free base in excess methanolic HCl solution and remove the solvent in vacuo to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851526
Source datasetuspto-grants-1989_07
ORD IDord-9ce88200164d4d8bb79a0337f4665721
Source noteuspto-grants-1989_07