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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981996Generated: November 4, 2026

1,3-Dihydroxynaphthalene → [(4-Hydroxy-2-naphthalenyl)oxy]acetic acid methyl ester

https://huagongshe.com/reaction/1981996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DihydroxynaphthaleneHCID 8601—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
SolventAcetoneHCID 180—
Product[(4-Hydroxy-2-naphthalenyl)oxy]acetic acid methyl esterHCID 5436712119%

Reaction Steps

A mixture of 1.5180 g of 1,3-dihydroxynaphthalene and 1.70 g of anhydrous potassium carbonate in 10 ml of anhydrous acetone was stirred at room temperature for 1 hour. Methyl bromoacetate (0.91 ml) was added and stirring at room temperature was continued for 50 hours. The solvent was removed in vacuo and the residue was acidified and extracted with ethyl acetate. The dried (magnesium sulfate) extract was concentrated in vacuo and the product was purified by high pressure liquid chromatography using 20% ethyl acetate-toluene to give 0.419 g (19% yield) of [(4-hydroxy-2-naphthalenyl)oxy]acetic acid methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04594442
Source datasetuspto-grants-1986_06
ORD IDord-43993baea89c4e8987bc427c778cade0
Source noteuspto-grants-1986_06