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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173896Generated: November 2, 2026

Hydrochloric Acid → Bis[2-(acryloyloxy)ethyl] benzene-1,3-dicarboxylate

https://huagongshe.com/reaction/2173896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsophthaloyl chlorideHCID 7451—
Reactant2-Hydroxyethyl acrylateHCID 13165—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
SolventPyridine tolueneHCID 22007288—
ProductBis[2-(acryloyloxy)ethyl] benzene-1,3-dicarboxylateHCID 57107493—

Reaction Steps

A 500 ml round-bottom flask was initially charged with 64.1 g of hydroxyethyl acrylate in 100 ml of pyridine/toluene (1:1, v/v) together with 0.1 g of 2,6-di-tert-butyl-4-methylphenol at 0° C., and 56.1 g of isophthaloyl chloride were slowly added dropwise. The mixture was stirred at room temperature until the hydroxyethyl acrylate content had fallen below 0.1%. Thereafter, the mixture was poured onto 0.5 l of ice-water and acidified with 1 N aqueous hydrochloric acid. The aqueous phase was extracted three times with 0.5 l each time of tert-butyl methyl ether. The organic phase was washed with 10% sodium hydrogencarbonate solution, dried over sodium sulfate and filtered. Another 0.1 g of 2,6-di-tert-butyl-4-methylphenol was added and the organic solvent was distilled off. The product was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09057950B2
Source datasetuspto-grants-2015_06
ORD IDord-8fb1806cc70d4ea5a3c34c0a96fc0b64
Source noteuspto-grants-2015_06