Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 2-(4-Acetamino-3-methylphenyl)benzonitrile | HCID 21468838 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 5(2-Cyanophenyl)indazole | HCID 21468844 | — |
Reaction Steps
2-(4-Acetamino-3-methylphenyl)benzonitrile (15.2 mmole, 3.8 g) was dissolved in 50 ml acetic acid and treated for 1 hour at room temperature with a stream of gaseous N2O5 generated by the addition of nitric acid to sodium nitrite. Benzene and brine were added to the reaction. The organic layer was separated, dried and warmed gently on a rotorvap (45° C.) for 1 hour. The solution was concentrated. Ether and saturated sodium bicarbonate were added. The organic phase was dried and concentrated. The residue was chromatographed over silica gel eluted with 50% ether in hexane to yield 240 mg of 5-(2-cyanophenyl)indazole. (MS)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05569768 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-33fb2d116eed4646adf4f64dbb69a22f |
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| Source note | uspto-grants-1996_10 |
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