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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439346Generated: November 1, 2026

Potassium Cyanide → 2-(4-Chlorophenyl)-4,5,6,7-tetrahydro-2h-indazol-3-amine

https://huagongshe.com/reaction/1439346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant2-ChlorocyclohexanoneHCID 13203—
Reactant(4-Chlorophenyl)hydrazineHCID 70624—
Reactant2-OxocyclohexanecarbonitrileHCID 220297—
CatalystAcetic AcidHCID 176—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
Product2-(4-Chlorophenyl)-4,5,6,7-tetrahydro-2h-indazol-3-amineHCID 20312173—

Reaction Steps

A mixture of 3.6 parts of 4-chlorophenylhydrazine and 2.0 parts of triethylamine in 20.0 parts of toluene was stirred at room temperature for fifteen minutes. To the mixture was added 2.5 parts of 2-cyanocyclohexanone, prepared from commercial 2-chlorocyclohexanone and potassium cyanide [von R. E. Meyer, Helv. Chim. Acta., 16, 1291 (1933)], and a few drops of acetic acid. After refluxing for two hours, followed by stirring at room temperature overnight, the reaction mixture was evaporated to remove toluene and was treated with water, extracted with diethyl ether, dried over anhydrous magnesium sulfate and concentrated. Recrystallization from ethanol/water gave 2.6 parts of the compound, m.p. 140°-142°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04059434
Source datasetuspto-grants-1977_11
ORD IDord-37a261251e604ed5adada10d7346342c
Source noteuspto-grants-1977_11