Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558307Generated: October 30, 2026

Dimethyl Sulfoxide → 3-Chloro-5-methyl-2,4-hexanedione

https://huagongshe.com/reaction/558307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant5-Methyl-2,4-hexanedione (enol)HCID 138984—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-Chloro-5-methyl-2,4-hexanedioneHCID 2194989235%

Reaction Steps

Chlorotrimethylsilane (13.4 ml, 105 mmol) was added dropwise to a stirred pale yellow solution of tetrabutylammonium iodide (566 mg, 1.53 mmol) in dry acetonitrile (100 ml) at room temperature under nitrogen. The resulting solution was cooled in ice and 5-methylhexane-2,4-dione (4.50 g, 35.1 mmol) and then dry dimethylsulphoxide (7.47 ml, 105 mmol) were added dropwise over 5 minutes producing a yellow solution which was allowed to warm slowly to room temperature with stirring over 1 hour. Tetrabutylammonium bromide (566 mg, 1.75 mmol) was then added in one portion and the reaction was stirred at room temperature for 2 hours. The mixture was diluted with water (200 ml), stirred for 10 min and then extracted with ether (3×100 ml). The combined ether layers were dried over magnesium sulphate, filtered and concentrated under reduced pressure to leave a yellow oil. The crude product was purified by flash column chromatography on silica gel eluting with pentane:ethyl acetate (98:2, by volume) to provide the title compound (2.00 g) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063044B2
Source datasetuspto-grants-2011_11
ORD IDord-308a9538e9804c4992abfce57f04526e
Source noteuspto-grants-2011_11