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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199834Generated: October 25, 2026

Ethylene Glycol → 1,3-Dioxolane, 2-(3-bromo-4-fluorophenyl)-

https://huagongshe.com/reaction/1199834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product1,3-Dioxolane, 2-(3-bromo-4-fluorophenyl)-HCID 1097776578.3%

Reaction Steps

A mixture of 3-bromo-4-fluorobenzaldehyde (45.7 g), ethylene glycol (27.39 g), p-toluenesulphonic acid (0.225 g) and dry toluene (110 cm3) was heated at the reflux temperature under a Dean and Stark trap. After 4.5 hours, approximately 12 cm3 of water had collected in the trap, and analysis of the reaction mixture by gas liquid chromatography indicated that no starting aldehyde was present. The cooled mixture was washed with sodium bicarbonate solution and brine, and dried over anhydrous magnesium sulphate. Evaporation of the solvent under reduced pressure gave a yellow oil, which was purified by distillation under reduced pressure to give 2-(3-bromo-4-fluorophenyl)-1,3-dioxolane (43.56 g), boiling point 68°-106° C. at 0.004 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902814
Source datasetuspto-grants-1990_02
ORD IDord-6834390c755846bbb3883e56d45b4227
Source noteuspto-grants-1990_02