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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210024Generated: October 26, 2026

Piperidine → 2-Nitro-5-(piperidin-1-yl)benzoic acid

https://huagongshe.com/reaction/2210024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-Chloro-2-nitrobenzoic acidHCID 17286—
SolventDimethylacetamideHCID 31374—
Product2-Nitro-5-(piperidin-1-yl)benzoic acidHCID 14459331—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-chloro-2-nitrobenzoic acid (13.7 g), piperidine (27 ml) and DMA (100 ml) was stirred and heated to 120° C. for 18 hours. The mixture was evaporated. The residue was dissolved in water and the solution was basified to pH10 by the addition of 2N aqueous sodium hydroxide solution. The solution was extracted with ethyl acetate. The aqueous layer was acidified to pH2 by the addition of concentrated hydrochloric acid and extracted with ethyl acetate. The organic layer was dried (MgSO4) and evaporated to give 2-nitro-5-piperidinobenzoic acid (16.25 g), m.p.130°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457105
Source datasetuspto-grants-1995_10
ORD IDord-4680114c0a014396afdb5c5fc66f4162
Source noteuspto-grants-1995_10