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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357356Generated: October 30, 2026

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

https://huagongshe.com/reaction/357356

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 1). 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840727
Source datasetuspto-grants-1998_11
ORD IDord-edb8e9a14ef14d5c9f4752f924f2f0a9
Source noteuspto-grants-1998_11