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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184507Generated: November 1, 2026

1,3-Dibromopropane → 1-[4-(3-Bromopropoxy)-3-methylphenyl]ethanone

https://huagongshe.com/reaction/2184507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
Reactant4'-Hydroxy-3'-methylacetophenoneHCID 70135—
SolventAcetonitrileHCID 6342—
Product1-[4-(3-Bromopropoxy)-3-methylphenyl]ethanoneHCID 9993319—

Reaction Steps

A mixture of 4-hydroxy-3-methylacetophenone (14.5 g, 96 mmol), K2CO3 (17.5 g, 144 mmol), and 1.3-dibromopropane (30 g, 144 mmol) in acetonitrile (400 ml) was heated at reflux for 6 hours. At the end of the reaction, the solvent was removed on a rotary evaporator, and the crude solid was extracted into dichloromethane (750 ml). The insolubles inorganics were filtered off. The dichloromethane solution was concentrated again to a crude oil (34.5 g). Purification was effected by flash chromatography over a silica gel column (SiO2, 150 g; eluted with 7:3 hexane:dichloromethane, 2 l; and then with dichloromethane 2 l). The material thus purified weighed 14.6 g (56%) and was recrystallized from ethanol gave analytically pure 1-[4-(3-bromopropoxy)-3-methylphenyl]ethanone, m.p.=59°-61° C. ANALYSIS: Calculated for C12H15BrO2: 53.15%C 5.58%H Found: 53.35%C 5.52%H

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-a3aa1698e54743c89afaceedad7bbb1f
Source noteuspto-grants-2002_06