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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441793Generated: November 1, 2026

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

https://huagongshe.com/reaction/1441793

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 numberUS07655689B2
Source datasetuspto-grants-2010_02
ORD IDord-fa2c232237404c3091eb4f726819c5a9
Source noteuspto-grants-2010_02