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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702135Generated: October 31, 2026

Ethylene Glycol → HCID 20504189, compound

https://huagongshe.com/reaction/1702135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2,4-Dichlorobenzyl 3-pyridyl ketoneHCID 13671239—
SolventO-XyleneHCID 7237—
ProductHCID 20504189HCID 20504189—

Reaction Steps

2.25 g of 2,4-dichlorobenzyl 3-pyridyl ketone, 2.2 g of p-toluenesulfonic acid monohydrate and 1.0 g of ethylene glycol are heated at reflux for 24 hours in 20 ml of xylene, the resulting water being separated in a water separator. The mixture is then cooled, poured into 2N sodium hydroxide and extracted with diethyl ether, the organic phase is dried over anhydrous sodium sulfate and the solvent is removed under reduced pressure. The crude product is purified by chromatography on silica gel with n-hexane/ethyl acetate (1:1) to yield 3-[2-(2,4-dichlorobenzyl)-1,3-dioxolan-2-yl]pyridine, which melts at 76°-78°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380544
Source datasetuspto-grants-1983_04
ORD IDord-5cbd657376cf4560bfb2c1a2029f29eb
Source noteuspto-grants-1983_04