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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392492Generated: October 25, 2026

1,3-Dimethyl-2-imidazolidinone → Anthraquinone

https://huagongshe.com/reaction/392492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantPotassium CarbonateHCID 11430—
Reactant9,10-Anthracenedione, 1-amino-2-chloro-4-hydroxy-HCID 75590—
ReactantN,N-Dibutyl-3-aminophenolHCID 601234—
SolventWaterHCID 962—
ProductAnthraquinoneHCID 6780—

Reaction Conditions

Temperature140 °C

Reaction Steps

One part by weight of 1-amino-2-chloro-4-hydroxyanthraquinone, 10 parts by weight of 1,3-dimethyl-2-imidazolidinone, 1.0 part by weight of potassium carbonate and 1.0 part by weight of N,N-di-n-butyl-m-aminophenol were mixed at room temperature, and then heated to 140° C. While this temperature was maintained, the reaction was conducted for 3 hours. The reaction mixture was then cooled to room temperature, charged into 90 parts by weight of water, and extracted with toluene. After the solution was separated, toluene was distilled off under reduced pressure, and the residue was purified through silica gel column chromatography to obtain an anthraquinone compound as coloring matter No. 9 (yield 90%) in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800674B2
Source datasetuspto-grants-2004_10
ORD IDord-3e59d5b30b05441bb33a290e341e3ebc
Source noteuspto-grants-2004_10