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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638669Generated: October 31, 2026

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

https://huagongshe.com/reaction/638669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
Reactant2,2'-Methylenebis(4-methyl-6-tert-butylphenol)HCID 8398—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxybromideHCID 24613—
SolventWaterHCID 962—
SolventHeptaneHCID 8900—
Product2-tert-Butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylateHCID 10905896.2%

Reaction Steps

To the same flask as used in Example 1 were added 340.51 g (1.0 mole) of 2,2'-methylenebis(6-tert-butyl-4-methylphenol), 72.06 g (1.0 mole) of acrylic acid, 400 g of n-heptane and 212.5 g (2.10 moles) of triethylamine. After replacing the air in the container with nitrogen, 200.7 g (0.70 mole) of phosphorus oxybromide was added dropwise with stirring. After completion of the dropwise addition, the reaction solution was kept at 80° C. for 1 hour. Thereafter, 500 g of water was added, and after cooling to room temperature, the deposited product was filtered off. The product obtained was washed with water until the washing became neutral to obtain 379.6 g of 2,2'-methylenebis(6-tert-butyl-4-methylphenol) monoacrylate as a white crystal. Melting point, 132°-134° C. Yield, 96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562281
Source datasetuspto-grants-1985_12
ORD IDord-acae4bef46044efd8a9c580df0cc4a21
Source noteuspto-grants-1985_12