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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106293Generated: October 30, 2026

Ethylene Glycol → 2-(2-Bromoethyl)-2-methyl-1,3-dioxolane

https://huagongshe.com/reaction/1106293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromobutan-2-oneHCID 12452734—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-(2-Bromoethyl)-2-methyl-1,3-dioxolaneHCID 11805619—

Reaction Steps

A mixture of 75 g of 4-bromo-2-butanone, 40 g of ethylene glycol, 250 mg of p-toluenesulfonic acid acid and 500 ml of toluene is refluxed for about 4-6 hours under a Dean-Stark water trap. The mixture is cooled, poured into ethyl acetate and dilute potassium carbonate solution. The organic layer is separated, washed with water, dried over sodium sulfate, stripped of solvent and the residue is distilled under reduced pressure to give the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04312994
Source datasetuspto-grants-1982_01
ORD IDord-5579699143fc4414b844206821a3455e
Source noteuspto-grants-1982_01