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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200215Generated: November 1, 2026

Acetone → 2,2-dimethyl-2H-1,3-benzodioxole

https://huagongshe.com/reaction/1200215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCatecholHCID 289—
Reactantp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product2,2-dimethyl-2H-1,3-benzodioxoleHCID 285869—

Reaction Steps

A mixture of catechol (55 g, 0.5 moles), acetone (150 ml), benzene (150 ml) and p-toluenesulfonic acid (15 mg) was refluxed in a Soxlet extractor containing 140 g of baked 4Å molecular sieves for 24 hours, as described in E. R. Cole, et al., Aust. J. Chem. 33, 675 (1980). The sieves were replaced with fresh sieves and refluxing continued for another 24 hours. The solvents were removed in vacuo and the residue was triturated with 1 liter of hexane. The light yellow solution was decanted and washed with 10% NaOH until the washes were colorless. The organic layer was dried (Na2SO4) and evaporated to 32.4 g (43%) of title compound as an oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904775
Source datasetuspto-grants-1990_02
ORD IDord-fa44636bc5c34bd3877bbfe92658731b
Source noteuspto-grants-1990_02