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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012368Generated: October 27, 2026

Ethylene Glycol → 4-(1,3-Dioxolan-2-yl)benzaldehyde

https://huagongshe.com/reaction/1012368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTerephthalaldehydeHCID 12173—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(1,3-Dioxolan-2-yl)benzaldehydeHCID 1182998868.5%

Reaction Steps

To 134 g of terephthalaldehyde and 62 g of ethylene glycol, was added 400 mL of toluene, and then was added thereto 2 g of p-toluenesulfonic acid, to conduct dehydration reaction under azeotropic conditions. After the time when the reaction of water stopped in the reaction, the reaction liquid was heated under reflux for another 2 hours, followed by cooling. The resultant reaction liquid was poured into an aqueous sodium bicarbonate solution. The organic phase was concentrated, and then purified by silica gel column chromatography (yield amount 122 g, and yield 68.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977491B2
Source datasetuspto-grants-2011_07
ORD IDord-b32dee2489974b3abde46615685393ef
Source noteuspto-grants-2011_07