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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1373128Erstellt: 26. Oktober 2026

5-Aminovaleric acid → 4-(2-Oxopiperidinomethyl)-nitrobenzene

https://huagongshe.com/reaction/1373128

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Aminovaleric acidHCID 138—
EduktHydrochloric AcidHCID 313—
Edukt4-NitrobenzaldehydeHCID 541—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt4-(2-Oxopiperidinomethyl)-nitrobenzeneHCID 18005657—

Reaktionsschritte

6.4 g (42 mmol) of 4-nitrobenzaldehyde are dissolved in 150 ml of methanol and combined with 4.9 g (42 mmol) of 5-aminovaleric acid and 1.8 g (29 mmol) of sodium cyanoborohydride. The mixture is stirred for 18 hours at ambient temperature and then carefully mixed with 20 ml of conc. hydrochloric acid. The solvent is eliminated in vacuo, the residue is taken up in water and extracted with dichloromethane. The residue obtained after evaporation is chromatographed on silica gel (dichloromethane/methanol, 4:1). A mixture of methyl 5-(4-nitrobenzylamino)-pentanoate and 4-(2-oxopiperidinomethyl)-nitrobenzene is obtained which is dissolved in 100 methanol and combined with 50 ml of 1 N sodium hydroxide solution. The mixture is stirred for one hour at ambient temperature, 50 ml of 1 N hydrochloric acid are added and the reaction solution is evaporated down to 100 ml. The aqueous phase thus obtained is extracted with dichloromethane. The combined organic phases are dried over sodium sulphate and evaporated to dryness.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07160901B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-3ee0601106844b04b779bf038b6cdf6e
Quellennotizuspto-grants-2007_01