Reacción #8729

ord-d3a94c6cd2a949a99cb74eb9ff971a3b

Ecuación de reacción

Cc1ccsc1
3-methylthiophene
ClCCl
dichloromethane
O=S(=O)(Cl)Cl
sulfuryl chloride
ClCCl
dichloromethane
O=S(=O)(O)Cl
chlorosulfonic acid
Cc1c(Cl)sc(Cl)c1S(=O)(=O)Cl
oil
Rendimiento 25.0%
Cc1c(Cl)sc(Cl)c1S(=O)(=O)Cl
2,5-Dichloro-4-methylthiophene-3-sulfonyl chloride
Rendimiento 25.0%

Condiciones de reacción

Temperatura
10°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction was concentrated
  2. 2
    workup.DISSOLUTIONredissolved in dichloromethane (30 mL)
  3. 3
    Temperaturacooled to −10° C
  4. 4
    TemperaturaThe reaction was maintained at −10° C. for 30 minutes
  5. 5
    workup.WAITat ambient temperature for 16 hours
  6. 6
    Extracciónextracted with dichloromethane (50 mL)
  7. 7
    SecadoThe organic layer was dried (Mg2SO4)
  8. 8
    Concentraciónconcentrated

Procedimiento

To a cooled (10° C.) solution of 3-methylthiophene (5 g, 50 mmol) in dichloromethane (15 mL) was added a solution of sulfuryl chloride (8.6 mL) in dichloromethane (5 mL). The reaction mixture was maintained at 10° C. for 30 minutes, then at ambient temperature for 16 hours. The reaction was concentrated and redissolved in dichloromethane (30 mL) and cooled to −10° C. To the cooled solution was added chlorosulfonic acid (2 mL, 100 mmol). The reaction was maintained at −10° C. for 30 minutes, then at ambient temperature for 16 hours, at which time it was poured into ice water (50 mL) and extracted with dichloromethane (50 mL). The organic layer was dried (Mg2SO4) and concentrated to furnish a brown oil (3.3 g, 25%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091204B2uspto-grants-2006_08