Reacción #172302

ord-8d9e6a3f48bc427483e6475ed283561b

Ecuación de reacción

Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
OCCCl
2-chloroethanol
Cc1ccc(S(=O)(=O)OCCCl)cc1
2-chloroethyl 4-methylbenzenesulfonate
Rendimiento 88.4%

Disolventes

Condiciones de reacción

Temperatura
2.5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe resulting mixture was extracted with ethyl acetate (3×100 mL)
  2. 2
    LavadoThe combined organic layers were washed with 1 N HCl (3×100 mL), water (100 mL×3)
  3. 3
    Secadodried (Na2SO4)
  4. 4
    Concentraciónconcentrated under reduced pressure

Procedimiento

In a typical run, p-toluenesulfonyl chloride (TsCl, 70.5 g, 0.37 mol) was added slowly to a solution of 2-chloroethanol (38; 25.0 g, 0.31 mol) in pyridine (100 mL) at 0° C. The reaction mixture was stirred at 0-5° C. for 18 h. Ice water (300 mL) was added and the resulting mixture was extracted with ethyl acetate (3×100 mL). The combined organic layers were washed with 1 N HCl (3×100 mL), water (100 mL×3), dried (Na2SO4) and concentrated under reduced pressure to afford 2-chloroethyl 4-methylbenzenesulfonate 39 (64.3 g, 88%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08846947B2uspto-grants-2014_09