HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → HCID 15434618, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | HCID 22125701 | HCID 22125701 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 15434618 | HCID 15434618 | 59.1% |
Reaction Steps
A mixture of 5-(4-fluorobenzoyl)-6-trifluoromethyl-sulfonyloxy-2-naphthalenesulfonamide (1.0 g, 2.1 mmol) [pre pared as described in step 2 above], potassium cyanide (0.15 mg, 2.3 mmol), and tetrakis(triphenylphosphine)palladium(0) in dioxane (15 ml) was heated at reflux under argon. After 2 h, the reaction mixture was cooled to RT, poured into brine, and the product was extracted into ethyl acetate. The organic layer was dried with sodium sulfate and concentrated in vacuo. The crude product was purified by flash chromatography (gradient elution, 20-50% ethyl acetate/hexane) and then recrystallized from ethyl acetate-hexane to give 0.44 g of 5-(4-fluorobenzoyl)-6-cyano-2-naphthalenesulfonamide as a white solid (54% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150397 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-d72d649b75454b248c92aa4576aed0a2 |
| Source note | uspto-grants-2000_11 |