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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587848Generated: October 27, 2026

4-(2-Bromoethyl)phenol → 2,2-diphenyl-5-[N-(4-hydroxyphenethyl)-N-methylamino]pentanamide

https://huagongshe.com/reaction/1587848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Bromoethyl)phenolHCID 84221—
ReactantSodium BicarbonateHCID 516892—
Reactant2,2-Diphenyl-5-methylaminopentanamideHCID 19088475—
SolventAcetonitrileHCID 6342—
Product2,2-diphenyl-5-[N-(4-hydroxyphenethyl)-N-methylamino]pentanamideHCID 19088513—

Reaction Steps

A mixture containing 2,2-diphenyl-5-methylaminopentanamide (0.36 g-see Preparation 3), 4-hydroxyphenethyl bromide (0.26 g), sodium bicarbonate (0.5 g) and acetonitrile (20 ml) was heated under reflux for 16 hours. The mixture was partitioned between dichloromethane (40 ml) and aqueous sodium bicarbonate (30 ml), the layers separated and the aqueous layer extracted with dichloromethane (2×30 ml). The combined dichloromethane extracts were concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with dichloromethane containing methanol (0% up to 10%). The product-containing fractions were combined and concentrated in vacuo to give a foam which was further purified by column chromatography on alumina eluting with dichloromethane containing methanol (0% up to 10%). The product-containing fractions were combined and concentrated in vacuo to give the title compound as a foam, yield 0.09 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05219871
Source datasetuspto-grants-1993_06
ORD IDord-b02eef37f69b4eb68ddee4f566cd4a8c
Source noteuspto-grants-1993_06