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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368209Generated: October 30, 2026

4-Chlorobenzylpiperazine → 1-(((4-Chlorobenzyl)amino)carbonyl)-4-(4-chlorobenzyl)piperazine

https://huagongshe.com/reaction/1368209

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylpiperazineHCID 134826—
Reactant1-Chloro-4-(isocyanatomethyl)benzeneHCID 3372379—
SolventTetrahydrofuranHCID 8028—
Product1-(((4-Chlorobenzyl)amino)carbonyl)-4-(4-chlorobenzyl)piperazineHCID 2226498054.4%

Reaction Steps

To a solution of 4-chlorobenzylisocyanate (0.59 g, 3.5 mmol) in anhydrous THF (15 mL) at 0° C. was added 1-(4-chlorobenzyl)piperazine (0.74 g, 3.5 mmol). The resultant mixture was stirred at ambient temperature. After 20 hours the mixture was concentrated of volatiles. The resulting solid was washed with ethyl acetate and dried in vacuo to afford 0.72 g of 1-(((4-chlorobenzyl)amino)carbonyl)-4-(4-chlorobenzyl)piperazine as a white solid; NMR (CDCl3) 7.4 (m, 4), 7.3 (m, 2), 7.2 (m, 2), 4.4-4.1 (m, 6), 3.6 (m, 4), 3.0 (m, 2) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573266B1
Source datasetuspto-grants-2003_06
ORD IDord-e14ae20502594e2a836253c1ef215c16
Source noteuspto-grants-2003_06