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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723656Generated: October 29, 2026

Acetone → 3,4-Dimethylhexane-2,5-dione

https://huagongshe.com/reaction/723656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant2,3,4,5-tetramethylfuranHCID 139198—
Product3,4-Dimethylhexane-2,5-dioneHCID 3285142.5%

Reaction Steps

Compound 219A was made in accordance with the procedures described in Hancock et al. J. Org. Chem. 42,1850–1856 (1977) & Amarnath et al. J. Org. Chem., 60, 301–307 (1995). 2-Propanone (100 mL, 1.1 mol) was refluxed over PbO2 (26.7 g, 0.112 mol) for 28 h. After cooling to rt, the reaction mixture was filtered and the residue was washed with acetone. The filtrate was concentrated under reduced pressure to remove the acetone and then distilled at 20 Torr. The fraction that came over between 100–120° C. was collected to give 6.75 g (42.5%) of 3,4-dimethylhexane-2,5-dione as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141578B2
Source datasetuspto-grants-2006_11
ORD IDord-1894c20ee7c1481da7af557f5cbf555e
Source noteuspto-grants-2006_11