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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466761Generated: November 3, 2026

Chloroacetone → 1-((3-Bromophenyl)thio)-2-propanone

https://huagongshe.com/reaction/1466761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
Reactantm-BromobenzenethiolHCID 80597—
ReactantDiisopropylethylamineHCID 81531—
SolventTetrahydrofuranHCID 8028—
Product1-((3-Bromophenyl)thio)-2-propanoneHCID 62804974—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromothiophenol (2.89 g, 15.29 mmol) and chloroacetone (1.278 mL, 16.06 mmol) were mixed in THF (80 mL) and cooled to 0° C. N,N-Diisopropylethylamine (6.65 mL, 38.23 mmol) was added and the reaction was stirred at 0° C. for five minutes then allowed to warm to room temperature and stirred overnight. The reaction was then extracted with EtOAc and H2O and the organic portion was concentrated to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000025B2
Source datasetuspto-grants-2015_04
ORD IDord-1a0f80a2f66e4fca87f886ee97193c7d
Source noteuspto-grants-2015_04