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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623662Generated: November 3, 2026

Potassium Hydroxide → 2-(Benzyloxy)-5-hydroxybenzoic acid

https://huagongshe.com/reaction/1623662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 5-{[(4-methylphenyl)sulfonyl]oxy}-2-[(phenylmethyl)oxy]benzoateHCID 86762539—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(Benzyloxy)-5-hydroxybenzoic acidHCID 24771944—

Reaction Steps

Methyl 5-{[(4-methylphenyl)sulfonyl]oxy}-2-[(phenylmethyl)oxy]benzoate (may be prepared as described in Description 75; 22.0 g, 53.3 mmol) was boiled with potassium hydroxide (20.95 g, 373 mmol) in a mixture of ethanol (320 ml) and water (80 ml) overnight. After the ethanol had been evaporated, the aqueous solution was washed with ethyl acetate (500 ml), and then acidified with concentrated HCl. The mixture was extracted with ethyl acetate. The organic phase was washed with saturated brine, dried over sodium sulfate, and evaporated in vacuo to yield the title compound as a yellow oil. 14 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-8be47d2d3bb046f5837edaf2085042dc
Source noteuspto-grants-2014_07