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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003755Generated: October 30, 2026

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

https://huagongshe.com/reaction/1003755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium CarbonateHCID 10340—
Reactant2-BromobenzaldehydeHCID 81129—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(4-Bromophenyl)-1,3-dioxolaneHCID 2773842—

Reaction Steps

40 g (216 mmol) of bromobenzaldehyde, 39 ml (700 mmol) of ethylene glycol, 1.6 g (9.3 mmol) of p-toluene sulphonic acid and 670 ml of toluene are introduced into a 2 l three-necked flask equipped with a Dean-Stark apparatus under nitrogen. The reaction mixture is taken to reflux whilst eliminating the water formed. After 24 hours of reflux, the reaction mixture is hydrolized with a saturated solution of sodium carbonate (240 ml). The organic phase is recovered and washed twice with a saturated solution of sodium chloride (2×160 ml), then concentrated under vacuum. The crude product obtained is distilled under 40 mm/Hg (150-156° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046352
Source datasetuspto-grants-2000_04
ORD IDord-a54c1747fabe4c7894f4cb9f42347a8e
Source noteuspto-grants-2000_04