Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938615Generated: November 1, 2026

Benzene → 5(2-Cyanophenyl)indazole

https://huagongshe.com/reaction/1938615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantNitric AcidHCID 944—
Reactant2-(4-Acetamino-3-methylphenyl)benzonitrileHCID 21468838—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventSodium chloride; waterHCID 57417360—
Product5(2-Cyanophenyl)indazoleHCID 21468844—

Reaction Conditions

Temperature45 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693633
Source datasetuspto-grants-1997_12
ORD IDord-de088c8441e246b59b7a9f4fced82974
Source noteuspto-grants-1997_12