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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604844Generated: October 26, 2026

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

https://huagongshe.com/reaction/604844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3'-BromoacetophenoneHCID 16502—
SolventBenzeneHCID 241—
Product2-(3-Bromophenyl)-2-methyl-1,3-dioxolaneHCID 10999218—

Reaction Steps

30.1 g (151 mmol) of (3-bromophenyl)methyl ketone and 13.8 g (222 mmol) of ethylene glycol are dissolved in 120 mL of benzene, mixed with 60 mg of 4-toluenesulphonic acid and boiled under reflux at a water separator (Dean-Stark apparatus) until no more water is separated off. The reaction solution is washed with 50 mL of a 0.5 M NaHCO3 solution, the organic phase is separated off and dried over anhydrous MgSO4. After removal of the benzene in a rotary evaporator, the residue becomes the product with a purity (GC) of 97% in nearly quantitative yield as colorless oily liquid. C10H11O2Br.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910744B2
Source datasetuspto-grants-2011_03
ORD IDord-f8b60560772c45c29d4319abe3ba1a7c
Source noteuspto-grants-2011_03