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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437657Generated: October 29, 2026

1-Benzyl-N-(2-nitrophenyl)piperidin-4-amine → N1-(1-benzylpiperidin-4-yl)benzene-1,2-diamine

https://huagongshe.com/reaction/437657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-N-(2-nitrophenyl)piperidin-4-amineHCID 81675—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductN1-(1-benzylpiperidin-4-yl)benzene-1,2-diamineHCID 93779—

Reaction Steps

A solution of 31 parts of N-(2-nitrophenyl)-1-(phenylmethyl)-4-piperidinamine in 160 parts of tetrahydrofuran is hydrogenated at normal pressure and at a temperature of 40° C, with 20 parts of Raney nickel catalyst. After the calculated amount of hydrogen is taken up (3 moles) hydrogenation is stopped. The catalyst is filtered off and from the filtrate the solvent is evaporated. The solid residue is washed with 160 parts of 2,2'-oxybispropane, to yield 22 parts of N-[1-(phenylmethyl)-4-piperidinyl]-1,2-benzenediamine; mp. 112°-113° C. On concentrating the filtrate to about one quarter of its volume a second crop of 2.5 parts of N-[1-(phenylmethyl)-4-piperidinyl]-1,2-benzenediamine is obtained; mp. 108°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-ddd0e36b20eb4268a92c4ef6cee40dd9
Source noteuspto-grants-1977_06