HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → 1-Amino-4-hydroxy-2-(4-fluorosulphonylphenoxy)anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Benzenesulfonyl chloride, 4-((1-amino-9,10-dihydro-4-hydroxy-9,10-dioxo-2-anthracenyl)oxy)- | HCID 87461 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Amino-4-hydroxy-2-(4-fluorosulphonylphenoxy)anthraquinone | HCID 19083397 | — |
Reaction Steps
To a mixture of 1-amino-4-hydroxy-2-(4-chlorosulphonylphenoxy)anthraquinone (2 parts) and 1,4-dioxane (25 parts), stirring at ambient temperature, was added a solution of potassium fluoride (0.6 parts) in water (5 parts). The mixture was heated to 60° C. and stirred at this temperature for 20 minutes. After cooling to 0°-5° C., the product was isolated by filtration, washed with water and dried at 50° C. to yield: 1-amino-4-hydroxy-2-(4-fluorosulphonylphenoxy)anthraquinone (1.6 parts). λmax=515.0 nm (CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05759211 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-18cdd58fa173405d9ecfc18d31e4984e |
| Source note | uspto-grants-1998_06 |