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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360484Generated: October 27, 2026

Propyl mercaptan → 4-(Propylthio)butan-2-one

https://huagongshe.com/reaction/1360484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyl mercaptanHCID 7848—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-2-butanoneHCID 80608—
SolventTetrahydrofuranHCID 8028—
Product4-(Propylthio)butan-2-oneHCID 1327528093.7%

Reaction Steps

Solid sodium hydride (60% dispersion in oil, 2.90 g, 72.3 mmol) was added in portions over 5 minutes to a stirred solution of 1-propanethiol (6.00 g, 78.8 mmol) in tetrahydrofuran (262 mL). After 15 minutes, a thick white suspension had formed. To the suspension was added 1-chloro-3-butanone (7.00 g, 65.7 mmol), which caused the reaction mixture to warm and a cloudy solution to form. After 30 minutes, the cloudy solution was partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the organic layer was washed with saturated aqueous sodium bicarbonate (100 mL) and brine (100 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford a pale brown oil. The crude product was purified by flash chromatography (silica gel, elution with 20% ethyl acetate in hexanes) to provide 9.0 g of 4-(propylthio)butan-2-one as a clear liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879849B2
Source datasetuspto-grants-2011_02
ORD IDord-4122fa9e865f4c29ac89dd0cde84d3b7
Source noteuspto-grants-2011_02