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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107107Generated: November 1, 2026

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

https://huagongshe.com/reaction/2107107

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 numberUS04933348
Source datasetuspto-grants-1990_06
ORD IDord-4a3048df2968494ba5819b8b8a32ccd3
Source noteuspto-grants-1990_06