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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252261Generated: October 27, 2026

Ethylene Glycol → 5-Bromo-1,1-(ethylenedioxo)-indane

https://huagongshe.com/reaction/2252261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantAmmoniaHCID 222—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5-Bromo-1-indanoneHCID 520695—
SolventBenzeneHCID 241—
Product5-Bromo-1,1-(ethylenedioxo)-indaneHCID 45158894—

Reaction Steps

A mixture of 5-bromo-1-indanone (13.0 g, 61.8 mmol), p-toluenesulfonic acid (23 mg, 0.12 mmol) and ethylene glycol (27.6 mL, 494.6 mmol) in benzene (140 mL) was refluxed for about 24 hours, using a Dean-Stark trap to remove water. The mixture was cooled, poured into excess 5% aqueous sodium bicarbonate and was extracted with toluene. The combined organic extracts were washed with brine, dried with MgSO4, filtered, and evaporated in vacuum. The residue was purified by flash column chromatography using dichloromethane as the mobile phase to give the above intermediate. MS (DCI/NH3): m/z 254, 256 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320986B2
Source datasetuspto-grants-2008_01
ORD IDord-89f48ed5b59a4f4195cf5a3d58126f1e
Source noteuspto-grants-2008_01