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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24928Generated: October 26, 2026

4-Nitrobenzaldehyde → 4-(Azetidin-1-yl-methyl)-nitrobenzene

https://huagongshe.com/reaction/24928

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantAzetidine hydrochlorideHCID 12308726—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product4-(Azetidin-1-yl-methyl)-nitrobenzeneHCID 22569653—

Reaction Steps

6.2 g (41 mmol) of 4-nitrobenzaldehyde and 3.8 g (40.6 mmol) of azetidine-hydrochloride are dissolved in 120 ml of ethanol. 2.6 g (41 mmol) of sodium cyanoborohydride are added at 0° C. The mixture is slowly heated to ambient temperature and then stirred for 18 hours. Then the solvent is eliminated in vacuo, the residue is taken up in ethyl acetate and washed with water. The solvent is eliminated in vacuo and after chromatography of the residue on silica gel (ethyl acetate/methanol/NH4OH=95:5:0.5) a light brown oil is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855710B2
Source datasetuspto-grants-2005_02
ORD IDord-ebebe92616344816b517ea4dc75ba6dd
Source noteuspto-grants-2005_02