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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019484Generated: October 27, 2026

1,5-Dichloroanthraquinone → 1,5-Bis((2-(dimethylamino)ethyl)(methyl)amino)anthracene-9,10-dione

https://huagongshe.com/reaction/1019484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DichloroanthraquinoneHCID 6711—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
SolventWaterHCID 962—
Product1,5-Bis((2-(dimethylamino)ethyl)(methyl)amino)anthracene-9,10-dioneHCID 59229118—

Reaction Steps

A mixture of 1,5-dichloroanthraquinone (5.5 g, 20 mmol) and N,N,N′-trimethylethylenediamine (40 ml) was refluxed for 18 h. The mixture was cooled to room temperature, diluted with water (400 mL) and extracted with chloroform (2×200 mL). The combined organic layer was washed with water, brine, dried over MgSO4 and evaporated to dryness. The residue thus obtained was purified by silica gel flash chromatography [CHCl3/MeOH/Et3N (44:5:1)] to provide Compound 9. Abs (max, PBS pH 7.4)=508 nm. The structure of Compound 9 is given below:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08715944B2
Source datasetuspto-grants-2014_05
ORD IDord-ac9cf472fe20486fb5e73b1f3619b2a4
Source noteuspto-grants-2014_05