Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735118Generated: October 31, 2026

4-Methylpiperidine → 1-(2-Chloro-4-nitrobenzyl)-4-methylpiperidine

https://huagongshe.com/reaction/735118

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpiperidineHCID 69381—
Reactantalpha,2-Dichloro-4-nitrotolueneHCID 3016511—
SolventEthyl AcetateHCID 8857—
Product1-(2-Chloro-4-nitrobenzyl)-4-methylpiperidineHCID 68816543—

Reaction Steps

1 g (4.85 mmol) of 2-chloro-4-nitrobenzylchloride is slowly added dropwise to 2 mL (16.22 mmol) of 4-methylpiperidine at ambient temperature and the mixture is stirred for 15 minutes. The reaction mixture is diluted with ethyl acetate and extracted twice with water. The organic phase is dried over sodium sulfate and evaporated down. Yield: 1.3 g (99.7% of theory); C13H17ClN2O2 (M=268.74); calc.: molecular ion peak (M+H)+: 269/271; found: molecular ion peak (M+H)+: 269/271; Rf value: 0.4 (Alox, petroleum ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592373B2
Source datasetuspto-grants-2009_09
ORD IDord-68fe302d281a4c348e1ddba06fb81b3a
Source noteuspto-grants-2009_09