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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,5-Dichloroanthraquinone | HCID 6711 | — |
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1-Chloro-5-(2-(dimethylamino)ethylamino)anthracene-9,10-dione | HCID 14320125 | 16.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334281B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-16fd1327c7c2454691174437859f1ca9 |
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| Source note | uspto-grants-2016_05 |
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