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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52045Generated: October 26, 2026

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

https://huagongshe.com/reaction/52045

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 numberUS05616582
Source datasetuspto-grants-1997_04
ORD IDord-e548eecaff784fc8846e4a93534b5491
Source noteuspto-grants-1997_04