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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417793Generated: October 25, 2026

Ethyl 4-((4-chloro-2-nitrophenyl)amino)piperidine-1-carboxylate → Ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/2417793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-((4-chloro-2-nitrophenyl)amino)piperidine-1-carboxylateHCID 104608—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylateHCID 104609—

Reaction Steps

A solution of 59 g of 1-carbethoxy-4-(2-nitro-4-chloroanilino)-piperidine in 270 ml of tetrahydrofuran and 96 ml of absolute ethanol was hydrogenated under normal pressure and at room temperature, using 15 g of Raney nickel as a catalyst. When the uptake of hydrogen had ended, the mixture was filtered and the filtrate was evaporated. Melting point: 150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04470989
Source datasetuspto-grants-1984_09
ORD IDord-cd3198adf58c421e8c4c8a6348df186c
Source noteuspto-grants-1984_09