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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381590Generated: November 2, 2026

4-Hydroxybenzyl Alcohol → Acetic acid, [4-(hydroxymethyl)phenoxy]-, ethyl ester

https://huagongshe.com/reaction/1381590

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantDimethylformamideHCID 6228—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
CatalystTetrabutylammonium BromideHCID 74236—
SolventEthyl AcetateHCID 8857—
ProductAcetic acid, [4-(hydroxymethyl)phenoxy]-, ethyl esterHCID 1141315763.8%

Reaction Steps

To a mixture of 2.00 g of p-hydroxybenzyl alcohol, 3.23 g of ethyl bromoacetate, 2.45 g of anhydrous potassium carbonate and 15 ml of N,N-dimethylformamide was added tetra-n-butylammonium bromide in a catalytic amount. The mixture was stirred at room temperature for 3 hours. The reaction mixture was diluted with ethyl acetate and insoluble matters were filtered off. The filtrate was washed with an aqueous sodium hydroxide solution and water, in this sequence. After drying over anhydrous magnesium sulfate, the solvent was distilled off. The residue was applied to silica gel column chromatography. Elution with a solvent mixture of hexane-ethyl acetate (3:2) gave 2.16 g of oily ethyl [p-(hydroxymethyl)phenoxy]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803211
Source datasetuspto-grants-1989_02
ORD IDord-60bc8b2da11a46c090dcda8b7365142f
Source noteuspto-grants-1989_02