Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522937Generated: October 25, 2026

1,5-Dichloroanthraquinone → 1-Chloro-5-(2-(dimethylamino)ethylamino)anthracene-9,10-dione

https://huagongshe.com/reaction/522937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DichloroanthraquinoneHCID 6711—
ReactantN,N-DimethylethylenediamineHCID 66053—
SolventDimethylacetamideHCID 31374—
Product1-Chloro-5-(2-(dimethylamino)ethylamino)anthracene-9,10-dioneHCID 1432012516.9%

Reaction Steps

A mixture of 1,5-dichloro anthraquinone (5.0 g, 18.0 mmol), N,N-dimethylacetamide (30 mL) and N,N-dimethylethylenediamine (2 mL, 18 mmol) was stirred at room temperature for 1 hour and then heated in an oil bath (T=100° C.) for 45 minutes. Reaction mixture was cooled and filtered. To the filtrate petroleum ether (50 mL) was added and combined mixture was stirred at 4° C. over night. Precipitated solid was removed by filtration and supernatant was evaporated to dryness, co-evaporated with chloroform and dried under vacuum. The crude dye was then purified on Biotage SP4 system using a gradient of methanol in chloroform. Appropriate fractions were combined and evaporated to dryness to provide Compound 17 (1.0 g) as a red solid. Rf (9:1 CHCl3/MeOH): 0.46; Abs (max, PBS)=500 nm. The structure of Compound 17 is given below:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334281B2
Source datasetuspto-grants-2016_05
ORD IDord-16fd1327c7c2454691174437859f1ca9
Source noteuspto-grants-2016_05