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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437104Generated: October 25, 2026

Hydroquinone → 4-(3,5-Di-t-butyl-4-hydroxyphenyl)-2-butyl methacrylate

https://huagongshe.com/reaction/437104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantMethyl MethacrylateHCID 6658—
Reactant4-(3,5-Di-t-butyl-4-hydroxyphenyl) butane-2-olHCID 21274350—
CatalystTitanium isopropoxideHCID 11026—
Product4-(3,5-Di-t-butyl-4-hydroxyphenyl)-2-butyl methacrylateHCID 2131787595%

Reaction Steps

A one-liter flask was charged with a mixture of 69.5 grams (0.25 mole) of 4-(3,5-di-t-butyl-4-hydroxyphenyl) butane-2-ol, 350 milliliters of methyl methacrylate, 0.5 gram of hydroquinone and 5 grams of tetraisopropyl titanate as the catalyst. The mixture was heated to reflux and a methanolmethylmethacrylate azeotrope slowly distilled off over a 3.5 hour period. The reaction flask was cooled slightly and 25 milliliters of water was added dropwise to hydrolyze the catalyst. The reaction mixture was allowed to cool to room temperature. The mixture was stirred 15 minutes longer and then filtered through diatomaceous earth. One hundred milliliters of hexane was added to the filtrate which separated into organic and inorganic phases. The organic phase containing the product in hexane was separated and dried over magnesium sulfate. The hexane was evaporated to obtain 82 grams (95 percent) of 4-(3,5-di-t-butyl-4-hydroxyphenyl)-2-butyl methacrylate. The boiling point of this compound was 150° C. to 155° C. at .15 milliliters of mercury pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04029713
Source datasetuspto-grants-1977_06
ORD IDord-f1bc98d48b9c4069b28d86475f96978e
Source noteuspto-grants-1977_06