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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681235Generated: October 27, 2026

Triethylamine → p-Ethoxalyloxyethylstyrene

https://huagongshe.com/reaction/1681235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxalyl chlorideHCID 20884—
Reactant2-(4-Vinylphenyl)ethanolHCID 22051832—
SolventBenzeneHCID 241—
Productp-EthoxalyloxyethylstyreneHCID 67847970—

Reaction Conditions

Temperature10 °C

Reaction Steps

A 200 ml flask equipped with a stirrer, a thermometer and a dropping funnel was charged with 14.8 g (0.1 mol) of p-hydroxyethylstyrene, 150 ml of benzene and 10.1 g (0.1 mol) of triethylamine and cooled to 10° C. To the mixture was added dropwise with stirring 13.7 g (0.1 mol) of ethoxalyl chloride for one hour at 10° C. to precipitate a hydrochloride of triethylamine (white solid). After mixing at room temperature for 2 hours, 80 g of hexane was added to complete precipitation of the hydrochloride. The hydrochloride is removed by filteration and the resultant filtrate was condensed to obtain the aimed compound. The compound was identified by 1H NMR (360 Mz) and IR. ##STR7##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169896
Source datasetuspto-grants-1992_12
ORD IDord-4bbf83498ecc416c991789cfb66783c8
Source noteuspto-grants-1992_12