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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2210024Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2210024

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt5-Chloro-2-nitrobenzoic acidHCID 17286—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2-Nitro-5-(piperidin-1-yl)benzoic acidHCID 14459331—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05457105
Quelldatensatzuspto-grants-1995_10
ORD IDord-4680114c0a014396afdb5c5fc66f4162
Quellennotizuspto-grants-1995_10