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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290432Generated: October 31, 2026

Acetone → [[8-Acetyl-7-[5-(4-acetyl-3-hydroxy-2-propylphenoxy)-pentyloxy]-2-naphthalenyl]oxy]acetic acid methyl ester

https://huagongshe.com/reaction/2290432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
Reactant1-[2,4-Dihydroxy-3-propylphenoxy]ethanoneHCID 20232737—
ReactantHCID 54389898HCID 54389898—
SolventDimethylformamideHCID 6228—
Product[[8-Acetyl-7-[5-(4-acetyl-3-hydroxy-2-propylphenoxy)-pentyloxy]-2-naphthalenyl]oxy]acetic acid methyl esterHCID 13505605—

Reaction Steps

A mixture of 1.66 g of [[8-Acetyl-7-(5-bromopentyloxy)-2-naphthalenyl]oxy]acetic acid methyl ester, 0.76 g of 1-[2,4-dihydroxy-3-propylphenoxy]ethanone and 0.81 g of anhydrous potassium carbonate in 30 ml of anhydrous acetone and 10 ml of anhydrous dimethylformamide was stirred at reflux. An additional 0.8 g of anhydrous potassium carbonate was added after 15 hours. Reflux was continued for a total of 22 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo to an oil which was treated with ether and water. The organic phase was separated and washed with 1N sodium hydroxide, water and sodium chloride solution. The black oil from concentration of the organic phase was purified by flash column chromatography to yield 1.45 g. mp 87°-89° (69%) of [[8-Acetyl-7 -[5-(4-acetyl-3-hydroxy-2-propylphenoxy)-pentyloxy]-2-napththalenyl]oxy]acetic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04616091
Source datasetuspto-grants-1986_10
ORD IDord-ec3cbda738574f6ea8c5963b93c0509a
Source noteuspto-grants-1986_10