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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861215Generated: October 26, 2026

Dimethylformamide → 2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-one

https://huagongshe.com/reaction/1861215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Ethylhexyl bromideHCID 86804—
Reactant2-HydroxybenzanthroneHCID 11242034—
SolventWaterHCID 962—
Product2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-oneHCID 22597178—

Reaction Steps

A 500 ml three neck flask was equipped with a mechanical stirrer, heating mantle and condenser. To the flask was added 25 g 2-hydroxy-7H-benzo[de]anthracene-7-one, 18 g powdered potassium carbonate, 25 g 2-ethylhexyl bromide and 250 g dimethylformamide (DMF). The mixture was heated to reflux. After seven hours, 4.5 g 2-ethylhexyl bromide was added and the mixture heated at reflux for an additional three hours. The mixture was then cooled to room temperature and 500 g deionized water was added. The solution was extracted twice with 200 g chloroform. The organic layers were combined and washed twice with 250 g water. The solvent was removed on a rotary evaporator, then the crude product was passed through a flash silica gel column using methylene chloride as the elutant. The product fractions were collected and the solvent removed using a rotary evaporator. The yield of 2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-one was 28.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531613B1
Source datasetuspto-grants-2003_03
ORD IDord-0a289f8628db4f4eb0a5878d1f23ca43
Source noteuspto-grants-2003_03