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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387702Generated: October 30, 2026

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

https://huagongshe.com/reaction/1387702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant4-BromobenzaldehydeHCID 70741—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product2-(4-Bromophenyl)-1,3-dioxolaneHCID 277384223,613.199%

Reaction Steps

A solution of 4-bromobenzaldehyde (5 g, 0.027 mol), ethylene glycol (7.0 g, 0.11 mmol), and p-toluenesulfonic acid (0.1 g, 0.5 mmol) in benzene was heated at reflux for 24 h using a Dean-Stark setup to remove water. The reaction was taken up in diethyl ether (100 mL) and washed with water (5×30 mL) and brine (30 mL). The organic phase was dried over magnesium sulfate and concentrated under vacuum to afford 2-(4′-bromophenyl)-1,3-dioxolane (5.95 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268513B1
Source datasetuspto-grants-2001_07
ORD IDord-608781426b45460a933b29f9937cb07c
Source noteuspto-grants-2001_07