Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22590Generated: October 25, 2026

Ethylene Glycol → 2-(3-Ethenylphenyl)-1,3-dioxolane

https://huagongshe.com/reaction/22590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantWaterHCID 962—
Reactant3-VinylbenzaldehydeHCID 39390—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventBenzeneHCID 241—
Product2-(3-Ethenylphenyl)-1,3-dioxolaneHCID 10241313—

Reaction Steps

To a solution of 3-ethenylbenzaldehyde from Step 1 (3.77 g) and ethylene glycol (1.8 mL) in benzene (40 mL) was added p-toluenesulfonic acid monohydrate (100 mg). The reaction mixture was heated to reflux for 6 hours. The water produced by the reaction was collected in a Dean-Stark trap. The reaction was allowed to cool to room temperature. The reaction was diluted with NH4OAc buffer and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated. Flash chromatography of the residue using 15% diethyl ether in hexane afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428171
Source datasetuspto-grants-1995_06
ORD IDord-587e164d49264c9ebf8e8b4e81762f69
Source noteuspto-grants-1995_06