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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250522Generated: October 26, 2026

Ethylene Glycol → 2-Methyl-2-(4-methylphenyl)-1,3-dioxolane

https://huagongshe.com/reaction/250522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantp-METHYLACETOPHENONEHCID 8500—
SolventTolueneHCID 1140—
Product2-Methyl-2-(4-methylphenyl)-1,3-dioxolaneHCID 275546979.1%

Reaction Steps

A mixture of 4-methylacetophenone (1.00 g, 7.45 mmol), p-toluenesulfonic acid (133 mg, 0.745 mmol) and ethylene glycol (1.20 mL, 22.4 mmol) in dry toluene (20 mL) was heated at reflux with a Dean-Stark apparatus under nitrogen for 24 h. The mixture was allowed to cool to room temperature and the solvent was evaporated in vacuo. The residue was taken up in ether (20 mL) and the solution was washed with saturated sodium bicarbonate solution (2×10 mL) and brine (1×10 mL), then dried (Na2SO4) and concentrated under reduced pressure. Flash column chromatography of the residue, eluting with 37% aqueous ammonia:ether:hexane (0.02:1:6) afforded 2-methyl-2-(4-methylphenyl)-1,3-dioxolane (23) as a colourless oil (1.05 g, 59%). 1H nmr (200 MHz, CDCl3) 1.65 (s, 3H, CH3), 2.35 (s, 3H, ArCH3), 3.74-3.86 (m, 2H, OCH2), 3.94-4.06 (m, 2H, OCH2), 7.15 (d, J=8.2 Hz, 2H, 2×ArH), 7.37 (d, J=8.2 Hz, 2H, 2×ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863313B2
Source datasetuspto-grants-2011_01
ORD IDord-125d60b86bf04bc18b8c7532c6023856
Source noteuspto-grants-2011_01