HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzylpiperazine → 1-(((4-Chlorobenzyl)amino)carbonyl)-4-(4-chlorobenzyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzylpiperazine | HCID 134826 | — |
| Reactant | 1-Chloro-4-(isocyanatomethyl)benzene | HCID 3372379 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(((4-Chlorobenzyl)amino)carbonyl)-4-(4-chlorobenzyl)piperazine | HCID 22264980 | 54.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06977258B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-ef0dbd696e9e48f286ba198edb9b6560 |
| Source note | uspto-grants-2005_12 |