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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007120Generated: October 28, 2026

1-(4-Nitrobenzyl)piperidine → 4-(Piperidin-1-ylmethyl)aniline

https://huagongshe.com/reaction/1007120

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrobenzyl)piperidineHCID 783541—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product4-(Piperidin-1-ylmethyl)anilineHCID 846150—

Reaction Steps

An acetic acid (3 ml) solution of the 4-nitrobenzylpiperidine compound (25) (65.8 mg, 0.2 mmol) obtained in the process 2 was added with zinc (300 mg) little by little at 0° C. After having been stirred at the room temperature for 2 hours, this was filtered to be taken out, had the solvent distilled out and neutralized with 2M aqueous sodium hydroxide, and then was extracted with ethylacetate. The resultant was washed with water and the saturated saline solution, dried and then vacuum concentrated, thus obtained a 4-aminobenzylpiperidine compound (26:R=2,2-dimethylcyclopropane) in the form of a yellow oily matter (50 mg, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794378B2
Source datasetuspto-grants-2004_09
ORD IDord-774164c333074fe0b96959aca8669aa9
Source noteuspto-grants-2004_09