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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915815Generated: November 1, 2026

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

https://huagongshe.com/reaction/915815

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), 4.44.1 (m, 6), 3.6 (m, 4), 3.0 (m, 2) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268140B2
Source datasetuspto-grants-2007_09
ORD IDord-a5c75e3731ae474782665501c6c73e9d
Source noteuspto-grants-2007_09