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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255608Generated: October 30, 2026

Ethylene Glycol → 4-Bromo-3-(1,3-dioxolan-2-yl)phenol

https://huagongshe.com/reaction/1255608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant2-Bromo-5-hydroxybenzaldehydeHCID 387179—
Catalystp-Toluenesulfonic acidHCID 6101—
CatalystPotassium CarbonateHCID 11430—
SolventTolueneHCID 1140—
Product4-Bromo-3-(1,3-dioxolan-2-yl)phenolHCID 5796870790.2%

Reaction Steps

A mixture of 2-bromo-5-hydroxybenzaldehyde (60.0 g, 299 mmol), ethylene glycol (56 mL, 1.00 mol), and p-toluenesulfonic acid (1.14 g, 5.98 mmol) in toluene (450 mL) was refluxed with Dean-Stark head for overnight. Potassium carbonate (3 g) was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried on anhydrous sodium sulfate. The solvent was removed under reduced pressure to give 4-bromo-3-(1,3-dioxolan-2-yl)phenol (66.1 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461135B2
Source datasetuspto-grants-2013_06
ORD IDord-1b6bb8887fac4b3ebbdc6ef8b1500897
Source noteuspto-grants-2013_06