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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638674Generated: October 31, 2026

Hydrochloric Acid → 2-tert-Butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylate

https://huagongshe.com/reaction/638674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2'-Methylenebis(4-methyl-6-tert-butylphenol)HCID 8398—
ReactantAcryloyl chlorideHCID 13140—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
Product2-tert-Butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylateHCID 10905894.7%

Reaction Steps

To a 500-ml four-necked flask equipped with a thermometer, stirring apparatus, condenser and dropping funnel were added 82.0 g (0.241 mole) of 2,2'-methylenebis(6-tert-butyl-4-methylphenol), 200 g of toluene and 23.9 g (0.290 mole) of triethylamine. After replacing the air in the container with nitrogen, 25 g (0.276 mole) of acryloyl chloride was added dropwise with stirring. After completion of the dropwise addition, stirring was continued for 1 hour, excess triethylamine was neutralized with a dilute hydrochloric acid and the formed triethylamine hydrochloride was then removed by washing with water. Toluene was then removed by evaporation from the toluene layer after completion of the washing, and the residue obtained was recrystallized from 20 g of n-hexane to obtain 90.0 g of 2,2'-methylenebis(6-tert-butyl-4-methylphenol) monoacrylate as a white crystal. Melting point, 132°-134° C. Yield, 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562281
Source datasetuspto-grants-1985_12
ORD IDord-5c626098b6624ff5ab4929555e564683
Source noteuspto-grants-1985_12