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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977708Generated: October 28, 2026

1-Bromo-3-chloropropane → 1-[4-((3-Chloropropyl)thio]-3-methoxyphenyl]ethanone

https://huagongshe.com/reaction/977708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantCyclohexaneHCID 8078—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Thio-3-methoxyphenyl)ethanoneHCID 21960101—
SolventAcetoneHCID 180—
Product1-[4-((3-Chloropropyl)thio]-3-methoxyphenyl]ethanoneHCID 10244271—

Reaction Steps

A mixture of 1-(4-thio-3-methoxyphenyl)ethanone (10.0 g, 54.9 mmol), potassium carbonate (9.0 g, 65.1 mmol), and acetone (100 ml) was stirred at reflux under nitrogen for 30 minutes. The reaction was cooled to ambient temperature and a solution of 1-bromo-3-chloropropane (6.5 ml, 9.5 g, 60.4 mmol) dissolved in acetone (25 ml) was dripped into the reaction. After complete addition, the reaction was heated to reflux and stirred under nitrogen for 17 hours. After the reaction was carried to substantial completion, the reaction mixture was filtered and the resulting filter cake was washed with acetone. The filtrate was concentrated to provide an amber oil. A small sample was solidified by trituration with hot cyclohexane to provide 1-[4-[(3-chloropropyl)thio]-3-methoxyphenyl]ethanone as a yellow solid, 11.7 g, m.p.=53°-55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614543
Source datasetuspto-grants-1997_03
ORD IDord-2c37971c21fa4acf8535fad61fab56c4
Source noteuspto-grants-1997_03