HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637586Generated: October 29, 2026
1,5-Dichloroanthraquinone → HCID 13558462, compound
https://huagongshe.com/reaction/637586
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Dichloroanthraquinone | HCID 6711 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-[(2-Hydrazinylethyl)amino]ethan-1-ol | HCID 13413808 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 13558462 | HCID 13558462 | 15.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04556654 |
|---|
| Source dataset | uspto-grants-1985_12 |
|---|
| ORD ID | ord-6f7a9a3bc05d4bf2a4544b0aa98aef78 |
|---|
| Source note | uspto-grants-1985_12 |
|---|