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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719418Generated: October 25, 2026

Acetyl chloride → 4-[(8-Acetyl-7-hydroxy-2-naphthalenyl)oxy]butanoic acid methyl ester

https://huagongshe.com/reaction/1719418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-[(7-Hydroxy-2-naphthalenyl)oxy]butanoic acid methyl esterHCID 13504781—
Solvent1,1-DichloroethaneHCID 6365—
Product4-[(8-Acetyl-7-hydroxy-2-naphthalenyl)oxy]butanoic acid methyl esterHCID 5440719929%

Reaction Steps

Under argon, 2.8 ml of acetyl chloride was added to a suspension of 5.15 g of aluminum chloride in 120 ml of dichloroethane and then 8 g of 4-[(7-hydroxy-2-naphthalenyl)oxy] butanoic acid methyl ester was added. The resulting mixture was stirred at room temperature for 30 minutes and at reflux for 16 hours. The solution was filtered and the dark residue was broken up with 3N hydrochloric acid and extracted with methylene chloride. The filtrate was combined with the methylene chloride extract, washed and dried to give a black oil which was purified by high pressure liquid chromatography, eluting with 2% ethyl acetate/toluene to yield 2.72 g, (29%) of 4-[(8-acetyl-7-hydroxy-2-naphthalenyl)oxy] butanoic acid methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539419
Source datasetuspto-grants-1985_09
ORD IDord-f5a421ef01d44e6da9cb935c11895ebb
Source noteuspto-grants-1985_09