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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378635Generated: October 25, 2026

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

https://huagongshe.com/reaction/1378635

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 numberUS05668156
Source datasetuspto-grants-1997_09
ORD IDord-1bd112727c634ae2aac890055ff5ab35
Source noteuspto-grants-1997_09