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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267987Generated: October 31, 2026

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

https://huagongshe.com/reaction/1267987

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), (m, 2), ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555537B2
Source datasetuspto-grants-2003_04
ORD IDord-ad555c4af99942f1a70d19c5bd62b9a9
Source noteuspto-grants-2003_04