HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → HCID 21400464, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 21400483 | HCID 21400483 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21400464 | HCID 21400464 | — |
Reaction Steps
30 g of 1-cyclohexylamino-4-chloro-6-nitroanthraquinone, 90 ml of p-tert.-butylaniline, 9.6 g of potassium acetate, 0.2 g of copperI chloride and 0.05 g of iodine are heated at 120°-130° C until only a little starting material remains detectable (approx. 12 hours being required). The mixture is diluted with 135 ml of methanol and the product is filtered off cold and washed with methanol and hot water. 26 g of 1-cyclohexylamino-4-(p-tert.-butylanilino)-6-nitroanthraquinone are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04056544 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-fcde85031ebc4f8fb7a2f1720713c40b |
| Source note | uspto-grants-1977_11 |