Reacción #531402

ord-5fc783b65e29403f9d035c6a663ed979

Ecuación de reacción

Clc1ccc(CN2CCNCC2)cc1
1-(4-chlorobenzyl)piperazine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
OCCCl
2-chloroethanol
ClCCN1CCN(Cc2ccc(Cl)cc2)CC1
title compound
Rendimiento 34.0%
ClCCN1CCN(Cc2ccc(Cl)cc2)CC1
1-(4-Chlorobenzyl)-4-(2-chloroethyl)piperazine
Rendimiento 34.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 61/2 hr
  2. 2
    Temperaturacooled
  3. 3
    Otrothe solvent removed in vacuo

Procedimiento

A mixture of 1-(4-chlorobenzyl)piperazine (21.05 g; 0.1 mole), anhydrous potassium carbonate (20.7 g; 0.15 mole) and 2-chloroethanol (8.85 g; 0.11 mole) in butanone (270 ml) was stirred at reflux for 61/2 hr, cooled, and the solvent removed in vacuo. Chromatography of the residue on silica eluting with chloroform gave 8.74 g (34%) of the title compound as an oil, νmax (film) 3350, 2910, 2800, 1595 cm-1 ; (Found; C, 61.48; H, 7.96; N, 10.13; C13H19N2ClO requires; C, 61.28; H, 7.52; N, 11.00%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04263299uspto-grants-1981_04