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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744496Generated: November 1, 2026

Water → 5-Amino-2-(piperidin-1-yl)benzonitrile

https://huagongshe.com/reaction/1744496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Nitro-2-(piperidin-1-yl)benzonitrileHCID 4811199—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product5-Amino-2-(piperidin-1-yl)benzonitrileHCID 1084575195.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

Ammonium chloride (1.6 g) and iron powder (8.4 g) were added to a mixed solvent of water (40 ml) and ethanol (120 ml), and the mixture was heated to 65° C. Then, 5-nitro-2-piperidinobenzonitrile (10 g) was added in parts over 20 min and the mixture was stirred at a refluxing temperature for 30 min. The reaction mixture was ice-cooled and filtrated. The solvent was evaporated under reduced pressure. To the residue was added aqueous sodium hydroxide solution, and the mixture was extracted with toluene. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, after which the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the residue to allow crystallization. The crystals were recrystallized from a mixed solvent of ethyl acetate-n-hexane to give the title compound (8.3 g), melting point: 148–149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015218B1
Source datasetuspto-grants-2006_03
ORD IDord-498b2d01b183472eacb1b5a4785b7b28
Source noteuspto-grants-2006_03