HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicarbonate Ion → Anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphonic acid, P-(3-aminophenyl)- | HCID 79477 | — |
| Reactant | 1-Amino-4-bromoanthraquinone | HCID 627326 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Water | HCID 962 | — |
| Product | Anthraquinone | HCID 6780 | 240.1% |
Reaction Steps
First of all, 17.3 g (0.1 mol) of 3-aminobenzenephosphonic acid was dispersed in a solution of 70 ml of water and 8 g of sodium hydroxide and mixed throughout. To the mixture, 8 g of sodim bicarbonate and 16 g (0.04 mol) of 1-amino-4-bromoanthraquinone were added and 0.6 g of copper chloride was then added and mixed at 70° to 75° C. until the reaction was terminated. The resultant mixture was filtered and the filtrate was made acidic to remove excess 3-aminobenzenephophonic acid. Sodium chloride was added to the filtrate and salted out, filtered and dried. It was then purified with alcohol to obtain a blue anthraquinone compound (20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05069719 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-1f06034151e64c81ad06986f5fa0d7dd |
| Source note | uspto-grants-1991_12 |