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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283807Generated: October 30, 2026

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

https://huagongshe.com/reaction/2283807

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 numberUS09145410B2
Source datasetuspto-grants-2015_09
ORD IDord-f7c6cf06c0284e6694eb3d72b9f21271
Source noteuspto-grants-2015_09