Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307869Generated: November 1, 2026

3-Bromopentane → N-(4-(2-ethyl-1-hydroxybutyl)phenyl)acetamide

https://huagongshe.com/reaction/2307869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopentaneHCID 15738—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-AcetamidobenzaldehydeHCID 73942—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-(2-ethyl-1-hydroxybutyl)phenyl)acetamideHCID 2260303552.2%

Reaction Steps

A solution of 3-bromopentane (0.331 mol) in (C2H5)2O (200 ml) was added dropwise to a solution of magnesium turnings (0.331 mol) in (C2H5)2O, the mixture was stirred at RT for 2 hours and then cooled to 0° C. A solution of N-(4-formyl-phenyl)acetamide (0.11 mol) in THF (400 ml) was added dropwise and the mixture was stirred for 10 minutes. The mixture was poured into aqueous NH4Cl and extracted with EtOAc. The organic layer was dried, filtered off and the solvent evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97/3/0.1). The pure fractions were collected and evaporated, yielding 13.5 g (52%) of (±)-N-[4-(2-ethyl-1-hydroxybutyl)phenyl]acetamide (interm. 13).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833375B2
Source datasetuspto-grants-2004_12
ORD IDord-5480ac7de9ea4cf784c922bbc955fe6b
Source noteuspto-grants-2004_12