Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814405Generated: November 2, 2026

Dibenzylamine → N,N-dibenzyl-3-chloropropan-1-amine

https://huagongshe.com/reaction/1814405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzylamineHCID 7656—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
SolventCyclohexaneHCID 8078—
ProductN,N-dibenzyl-3-chloropropan-1-amineHCID 1848253%

Reaction Steps

To a stirred suspension of K2CO3 (200 g, 1.5 mole) in cyclohexane 200 mL and 1-bromo-3-chloropropane (540 gms, 3.4 mole) is added dropwise over a period of 1 h at 20° C. dibenzyl amine (442 g, 2.24 mole). After complete addition the reaction is allowed to stir for an additional 20 h. The crude reaction mixture is filtered and then washed with saturated NaCl (3×100 mL). The organic phase is extracted with 3N HCl (3×100 mL). The resulting aqueous phase, containing the desired product as the hydrochloric salt, is washed with hexanes (3×100 mL) to remove any residual BCP. The aqueous phase is subsequently basified with 50 wt % NaOH and extracted with cyclohexane (3×100 mL). After solvent removal 324 g (53% yield) of the title compound was isolated as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875876B2
Source datasetuspto-grants-2005_04
ORD IDord-aed72395e34b4800bb554b4106b0085a
Source noteuspto-grants-2005_04