Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 23677017 | HCID 23677017 | — |
Reaction Steps
6.6 g (0.06 mol) of p-aminophenol in 4.0 g (0.06 mol) potassium hydroxide (purity 85%) and 80 ml of dimethylsulfoxide was heated under stirring. The water generated was distilled off under reduced pressure to obtain the potassium p-aminophenolate. To the solution, which was allowed to be cooled to room temperature, was added a solution of 10.9 g (0.06 mol) of 6-fluoro-2-chloroquinoxaline dissolved in 60 ml of dioxane. The mixture was reacted at 50°-60° C. for 3 hours. After the reaction was over, the reaction solution was poured onto ice and the separated solid was filtered off, and washed with 5% aqueous solution of sodium hydroxide and then washed with water. The substance thus obtained was recrystallized from ethanol to yield 8.2 g (yield 54%) of the intended compound (Compound No. 4) having a melting point of 174°-175.5° C. as light-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04376202 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-8e87a6baf3914dafa3fd0dd21a6d8836 |
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| Source note | uspto-grants-1983_03 |
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