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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830563Generated: October 31, 2026

Ethylene Glycol → HCID 12337274, compound

https://huagongshe.com/reaction/1830563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant3-Bromo-1-benzofuran-2-carbaldehydeHCID 12337272—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventBenzeneHCID 241—
SolventSodium BicarbonateHCID 516892—
ProductHCID 12337274HCID 12337274100.5%

Reaction Steps

3-bromo-1-benzofuran-2-carbaldehyde (5.49 g, 24.4 mmol) is combined with para-toluene sulfonic acid hydrate (232 mg, 1.2 mmol) and ethylene glycol (2.44 ml, 43.9 mmol) in benzene (75 ml). The reaction is refluxed with a Dean-Stark trap for 5 h. The mixture is cooled to rt and diluted with saturated NaHCO3 solution (20 ml) and left to stir for an additional 12 h. The layers are allowed to separate, and the organic layer is dried over Na2SO4, filtered, and concentrated to afford 6.6 g (100%) of 3-bromo-2-(1,3-dioxolan-2-yl)-1-benzofuran as a dark brown oil. HRMS (FAB) calcd for C11H9BrO3+H: 268.9814, found 268.9821.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067515B2
Source datasetuspto-grants-2006_06
ORD IDord-8afef1419604449ea0fc31f051252fd0
Source noteuspto-grants-2006_06