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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489205Generated: October 25, 2026

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

https://huagongshe.com/reaction/489205

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 numberUS06977258B2
Source datasetuspto-grants-2005_12
ORD IDord-ef0dbd696e9e48f286ba198edb9b6560
Source noteuspto-grants-2005_12