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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079351Generated: October 27, 2026

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

https://huagongshe.com/reaction/1079351

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 numberUS05580870
Source datasetuspto-grants-1996_12
ORD IDord-d93b6e40682649339e2f5f6501b5933a
Source noteuspto-grants-1996_12