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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487191Generated: October 26, 2026

Ethylene Glycol → 2-(5-Chloro-2-nitrophenyl)-1,3-dioxolane

https://huagongshe.com/reaction/1487191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant5-Chloro-2-nitrobenzaldehydeHCID 81123—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product2-(5-Chloro-2-nitrophenyl)-1,3-dioxolaneHCID 26738590.2%

Reaction Steps

In a flask equipped with a Dean-Stark water separator, 5-chloro-2-nitrobenzaldehyde (12.0 g, 64.7 mmol), ethylene glycol (8.0 g, 129.3 mmol) and p-toluenesulfonic acid (0.2 g) were dissolved in toluene (150 mL). The mixture was stirred at reflux for 8 hours. Dichloromethane was added and the organic phase was washed with saturated sodium bicarbonate and brine, then dried over anhydrous sodium sulfate, evaporated and purified by silica gel chromatography to afford the product 2-(5-chloro-2-nitrophenyl)-1,3-dioxolane (13.4 g, yield 90.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428508B2
Source datasetuspto-grants-2016_08
ORD IDord-3628717df63f43608aef6ebf813b0d85
Source noteuspto-grants-2016_08