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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744507Generated: November 1, 2026

Water → Ethyl 1-(4-amino-2-cyanophenyl)-4-piperidinecarboxylate

https://huagongshe.com/reaction/1744507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 1-(2-cyano-4-nitrophenyl)piperidine-4-carboxylateHCID 9280152—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
ProductEthyl 1-(4-amino-2-cyanophenyl)-4-piperidinecarboxylateHCID 2222790077.9%

Reaction Conditions

Temperature65 °C

Reaction Steps

Ammonium chloride (2.1 g) and iron powder (11.1 g) were added to a mixed solvent of water (110 ml) and ethanol (30 ml), and the mixture was heated to 65° C. Then, ethyl 1-(4-nitro-2-cyanophenyl)piperidin-4-ylcarboxylate (17.1 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 (12 g), melting point: 98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015218B1
Source datasetuspto-grants-2006_03
ORD IDord-d341ca4ff14f4215998ab865c22c16c5
Source noteuspto-grants-2006_03