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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637586Generated: October 29, 2026

1,5-Dichloroanthraquinone → HCID 13558462, compound

https://huagongshe.com/reaction/637586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DichloroanthraquinoneHCID 6711—
ReactantPotassium BicarbonateHCID 516893—
ReactantPotassium FluorideHCID 522689—
Reactant2-[(2-Hydrazinylethyl)amino]ethan-1-olHCID 13413808—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 13558462HCID 1355846215.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 11.1 g (40 mmol) of 1,5-dichloro-9,10-anthracenedione, 13.1 g (110 mmol) of 2-[(hydrazinoethyl)amino]ethanol, 4 g of anhydrous potassium bicarbonate, 1 g of anhydrous potassium fluoride, and 110 ml of dimethyl sulfoxide is stirred at 70° C. overnight. The mixture is chilled and the solids are collected by filtration, washed with water, then thoroughly with acetonitrile to give a residue that is crystallized from 2-propanol to leave 2.6 g of product. The hydrochloride salt is prepared as described in Example 3; mp 272°-273° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556654
Source datasetuspto-grants-1985_12
ORD IDord-6f7a9a3bc05d4bf2a4544b0aa98aef78
Source noteuspto-grants-1985_12