Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833297Generated: November 3, 2026

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

https://huagongshe.com/reaction/1833297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitro-2-piperidin-1-yl-benzoic acidHCID 2942421—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-Amino-2-piperidin-1-yl-benzoic acidHCID 808777—

Reaction Steps

30 Grams 2-chloro-5-nitrobenzoic acid was added in portions to 150 ml piperidine. The temperature of the reaction was allowed to rise during the addition. After the addition was complete, the reaction was heated at reflux temperature for two hours. The hot reaction mixture was poured into ice water, made acid by the addition of concentrated HCl until precipitation of the product was complete and filtered. The filter cake was recrystallized from ethanol to give 30.4 grams 5-nitro-2-piperidinobenzoic acid. m.p. = 201°-203° C. The nitro compound was reduced catalytically in ethanol with 5% palladium on carbon catalyst to give 5-amino-2-piperidinobenzoic acid. m.p. = 232°-235° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066457
Source datasetuspto-grants-1978_01
ORD IDord-b6e5204671554d718f65b87bcb2f4b47
Source noteuspto-grants-1978_01