HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256276Generated: October 25, 2026
1,5-Dichloroanthraquinone → 1,5-Bis(4-cyclohexylphenylamino)-anthraquinone
https://huagongshe.com/reaction/256276
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,5-Dichloroanthraquinone | HCID 6711 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | 4-Cyclohexylbenzenamine | HCID 80764 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,5-Bis(4-cyclohexylphenylamino)-anthraquinone | HCID 20163330 | — |
Reaction Steps
In a round bottom flask equipped with stirrer, thermometer, and nitrogen inlet is added 2.77 g (0.1M) 1,5-bischloroanthraquinone and 3.5 g (0.2M) of 4-cyclohexylaniline. 3.0 g anhydrous sodium acetate and 0.1 g anhydrous copper acetate are added as acid acceptor and reaction catalyst respectively. 50 g nitrobenzene are added and the stirred mass is heated to reflux under nitrogen atmosphere. The reaction is allowed to proceed for two hours at 185° C. Upon cooling, 50 g methanol is added and the crude dye separated by vacuum filtration. Subsequent purification by recrystalization and chromatography from alumina using toluene as the elvent affords the magneta pleochroic dye 1,5-bis(4-cyclohexylphenylamino)-anthraquinone. The optical order parameter was measured as 0.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04702561 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-8d56c5b5a35a4fcda4c347d4ddb3d7c7 |
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| Source note | uspto-grants-1987_10 |
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