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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756457Generated: October 26, 2026

4-Hydroxybenzyl Alcohol → 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenol

https://huagongshe.com/reaction/1756457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant3-Tert-butyl-4-methoxybenzoyl chlorideHCID 13633555—
SolventTetrahydrofuranHCID 8028—
Product4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenolHCID 21474530—

Reaction Steps

1.24 g (0.01 mol) of 4-hydroxybenzenemethanol, 1 ml (0.01 mol) of pyridine and 50 ml of THF are introduced into a round-bottomed flask. While cooling in an icebath, a solution of 2.2 g (0.01 mol) of 3-tert-butyl-4-methoxybenzoyl chloride in 50 ml of THF is introduced dropwise and the mixture is stirred at room temperature for 24 h. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column and eluted with a mixture of dichloromethane and ethyl ether (97:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439925
Source datasetuspto-grants-1995_08
ORD IDord-fdee8a17006349d9bc2ec8e965ec33c7
Source noteuspto-grants-1995_08