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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163396Generated: October 25, 2026

Acetone → HCID 13090997, compound

https://huagongshe.com/reaction/2163396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 7-hydroxy-4-oxo-4H-chromen-2-carboxylateHCID 5376802—
Reactant2-(3-Bromopropoxy)propylbenzeneHCID 22753563—
SolventChloroformHCID 6212—
ProductHCID 13090997HCID 13090997—

Reaction Steps

A mixture of 58.5 parts of ethyl 7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylate, 64.25 parts of 2-(3-bromopropoxy)propylbenzene, 17.25 parts of anhydrous potassium carbonate and 1000 parts of acetone was refluxed, with stirring, for 21/2 days and the hot solution filtered. The residue was washed with hot acetone and the combined filtrates evaporated to give an oil which was dissolved in chloroform. The resulting solution was washed with 1N sodium hydroxide solution and then dried. Evaporation of the chloroform gave an oil which yielded a solid on crystallisation from ethanol. The solid was chromatographed on silica gel, eluting with a 1:1 mixture of ethyl acetate and 40/60 light petroleum ether. Evaporation of the eluent and crystallisation of the resulting residue from ethanol gave 18.4 parts of ethyl 4-oxo-7-(3-[2-propylphenoxy]-propoxy)-4H-1-benzopyran-2-carboxylate, m.pt. 75°-76.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04133889
Source datasetuspto-grants-1979_01
ORD IDord-43929a1badc949f5aa957ee9cdda696f
Source noteuspto-grants-1979_01