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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989400Generated: October 26, 2026

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

https://huagongshe.com/reaction/989400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminovaleric acidHCID 138—
ReactantHydrochloric AcidHCID 313—
Reactant4-NitrobenzaldehydeHCID 541—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-(2-Oxopiperidinomethyl)-nitrobenzeneHCID 18005657—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638965B2
Source datasetuspto-grants-2003_10
ORD IDord-adad6317555d4b43af75bdbd03907a49
Source noteuspto-grants-2003_10