Reacción #8728

ord-2f30ba84e4194cd6b9cb4784c4f11ab7

Ecuación de reacción

O=S(=O)(Cl)c1cc(Cl)sc1Cl
2,5-dichlorothiophene-3-sulfonyl chloride
[S]Cl
sulfur monochloride
O
water
O=S(=O)(Cl)c1c(Cl)sc(Cl)c1Cl
solid
O=S(=O)(Cl)c1c(Cl)sc(Cl)c1Cl
2.4.5-Trichloro-thiophene-3-sulfonyl chloride

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added dropwise
  2. 2
    TemperaturaThe reaction was heated at 60° C. for an additional 3 hours, at which time it
  3. 3
    Temperaturato cool to ambient temperature
  4. 4
    Extracciónthe reaction extracted with dichloromethane (2×20 mL)
  5. 5
    LavadoThe combined organic layers were washed with saturated sodium bicarbonate solution
  6. 6
    Secadodried (Mg2SO4)
  7. 7
    Concentraciónconcentrated

Procedimiento

A mixture of 2,5-dichlorothiophene-3-sulfonyl chloride (1.2 g, 5 mmol) and sulfur monochloride (10 mg) in sulfuryl chloride (500 mg) was heated at 60° C. for 30 min, at which time was added dropwise a mixture of aluminum trichloride (10 mg) in sulfuryl chloride (500 mg). The reaction was heated at 60° C. for an additional 3 hours, at which time it was allowed to cool to ambient temperature. Cold water (20 mL) was added and the reaction extracted with dichloromethane (2×20 mL). The combined organic layers were washed with saturated sodium bicarbonate solution, dried (Mg2SO4) and concentrated to furnish a tan solid (420 mg, 33%).

Fuente

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