Reacción #1726669

ord-ce97125950ee49cb92d2c881177bc3e6

Ecuación de reacción

Br
hydrogen bromide
O=S(c1ccc(Cl)cc1)c1ccc(Cl)cc1
di(4-chlorophenyl)sulfoxide
C[Si](C)(C)Cl
trimethylchlorosilane
Clc1ccc(Br)cc1
4-bromochlorobenzene
Clc1ccc([S+](c2ccc(Cl)cc2)c2ccc(Cl)cc2)cc1.[Br-]
tris(4-chlorophenyl)sulfonium Bromide

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrokept at 0 to 5° C.
  2. 2
    workup.ADDITIONwas added dropwise over the period of 30 min into the reaction vessel
  3. 3
    workup.STIRRINGAfter agitated for one hr at 0° C.
  4. 4
    workup.WAITfollowed by another hr
  5. 5
    workup.ADDITIONagitation at room temperature, the reaction solution was slowly poured into an aqueous solution
  6. 6
    Extracciónextracted with 250 ml dichloromethane
  7. 7
    SecadoThe extract was dried with sodium sulfate

Procedimiento

Under a nitrogen atmosphere, 16.3 g (0.06 mol) of di(4-chlorophenyl)sulfoxide was dissolved in 250 ml dichloremethane. Into the resulting solution kept at 0 to 5° C., 10.8 g (0.10 mol) of trimethylchlorosilane was added dropwise; the mixture was stirred at 0° C. for 30 min. Thereafter, 200 g of a tetrahydrofuran (THF) solution of the Grignard reagent prepared by the usual process with 4-bromochlorobenzene (0.18 mol) was added dropwise over the period of 30 min into the reaction vessel cooled with 0 to 10° C. ice water. After agitated for one hr at 0° C., followed by another hr agitation at room temperature, the reaction solution was slowly poured into an aqueous solution containing 250 ml of an aqueous 12% hydrogen bromide solution and ice, then extracted with 250 ml dichloromethane. The extract was dried with sodium sulfate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08110337B2uspto-grants-2012_02