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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094988Generated: November 2, 2026

2-Nitro-5-piperidin-1-yl-benzoic acid ethyl ester → 2-Amino-5-piperidin-1-yl-benzoic acid ethyl ester

https://huagongshe.com/reaction/1094988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitro-5-piperidin-1-yl-benzoic acid ethyl esterHCID 66638963—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventMethanolHCID 887—
Product2-Amino-5-piperidin-1-yl-benzoic acid ethyl esterHCID 61306567—

Reaction Steps

Subsequently, crude 2-nitro-5-piperidin-1-yl-benzoic acid ethyl ester (3.8 g) was dissolved in methanol (35 ml), and platinum oxide (300 mg) was added to the solution at room temperature. The air in the reaction system was replaced by hydrogen, and the mixture was then stirred for 12 hr. After the completion of the reaction, the atmosphere in the reaction system was replaced by nitrogen, and the reaction solution was then filtered through Celite to remove platinum oxide, and was then concentrated under the reduced pressure to give crude 2-amino-5-piperidin-1-yl-benzoic acid ethyl ester (compound A) as a useful intermediate (3.4 g, crude yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-67cc1112fd4f4c8e9bd791a2a0be7b7d
Source noteuspto-grants-2012_03