Reacción #302890

ord-6d25758682194a3e9cb055f2726f3e52

Ecuación de reacción

NCc1cccc(Cl)c1Cl
2,3-dichlorobenzylamine
S=C=NCCCl
2-chloroethylisothiocyanate
Cl.Clc1cccc(CNC2=NCCS2)c1Cl
title compound
Rendimiento 163.2%
Cl.Clc1cccc(CNC2=NCCS2)c1Cl
((2,3-dichlorophenyl)methyl)-1,3-thiazolin-2-ylamine hydrochloride
Rendimiento 163.2%

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas placed in a sealed reaction vial
  2. 2
    Temperaturato cool
  3. 3
    Otroa solid precipitate that had formed
  4. 4
    Filtraciónwas collected by filtration
  5. 5
    LavadoThe solid was rinsed with diethyl ether
  6. 6
    Otrowas dried under reduced pressure

Procedimiento

A mixture of 0.5 gram (0.0028 mole) of 2,3-dichlorobenzylamine and 0.27 gram (0.0081 mole) of 2-chloroethylisothiocyanate in 10 mL of 1,4-dioxane was placed in a sealed reaction vial. The reaction mixture was heated to 80° C. where it stirred for about 18 hours. The reaction mixture was allowed to cool and a solid precipitate that had formed was collected by filtration. The solid was rinsed with diethyl ether and was dried under reduced pressure to yield 0.68 gram of the title compound. The NMR spectrum was consistent with the proposed structure.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08193118B2uspto-grants-2012_06