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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082635Generated: November 3, 2026

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

https://huagongshe.com/reaction/1082635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Hydroxy-3-(methylthio)phenyl)ethan-1-oneHCID 3017662—
SolventAcetonitrileHCID 6342—
Product1-[4-(3-Bromopropoxy)-3-methylmercaptophenyl]ethanoneHCID 10040638—

Reaction Steps

A mixture of 1-[4-hydroxy-3-(methylmercapto)phenyl]-ethanone (5.4 g; 30 mmol), K2CO3 (4.2 g), 1,3-dibromopropane (8 g, 39 mmol) in acetonitrile (150 ml) was heated at reflux for 3 hours and stirred at room temperature overnight. Acetonitrile was removed at reduced pressure and the residue was extracted into dichloromethane (250 ml). Insolubles were filtered off. The dichloromethane solution was concentrated. The crude product was purified on a silica gel column (SiO2, 100 g; eluted with 3:2 hexane:dichloromethane, 1.6 l). The compound crystallized upon concentration, and the product (3.5 g, 39%) was recrystallized from ethanol (40 ml) to yield 1-[4-(3-bromopropoxy)-3-(methylmercapto)phenyl]ethanone as white needles, 2.0 g; m.p.=120°-122° C. ANALYSIS: Calculated for C12H15BrO2S: 47.53%C 4.99%H Found: 47.74%C 4.91%H

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589495
Source datasetuspto-grants-1996_12
ORD IDord-3ae674454d194ac8916c69ec657f21d7
Source noteuspto-grants-1996_12