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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396883Generated: October 29, 2026

1-(2-(6-Nitrotetralin-1-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine → 1-(2-(6-Aminotetralin-1-yl) ethyl)-4-(3,4-dimethoxyphenyl)piperidine

https://huagongshe.com/reaction/2396883

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-(6-Nitrotetralin-1-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidineHCID 18986586—
SolventMethanolHCID 887—
Product1-(2-(6-Aminotetralin-1-yl) ethyl)-4-(3,4-dimethoxyphenyl)piperidineHCID 22362101—

Reaction Steps

A suspension of 3.2 g of 1-(2-(6-nitrotetralin-1-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine in 50 ml of methanol is hydrogenated in the presence of 1.6 g of Pd/C (5%) until the absorption of hydrogen has come to a standstill. The catalyst is filtered off, and the filtrate is worked up in the customary manner and gives 1-(2-(6-aminotetralin-1-yl) ethyl)-4-(3,4-dimethoxyphenyl)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05495022
Source datasetuspto-grants-1996_02
ORD IDord-635128aeb4064d568739f15449e11af7
Source noteuspto-grants-1996_02