Reacción #640565

ord-991224432001483c93a0aff8422aef27

Ecuación de reacción

Cl
hydrochloric acid
[Mg]
magnesium
Clc1ccccc1
chlorobenzene
C[Si](C)(C)Cl
trimethylsilyl chloride
O=S(c1ccccc1)c1ccccc1
Diphenyl sulfoxide
[Cl-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium chloride

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added dropwise at a temperature below 20° C
  2. 2
    workup.WAITThe reaction solution was aged for one hour
  3. 3
    Otroto quench
  4. 4
    Otrothe reaction
  5. 5
    OtroThe water layer was separated
  6. 6
    Lavadowashed with 100 g of diethyl ether

Procedimiento

Diphenyl sulfoxide, 40 g (0.2 mole), was dissolved in 400 g of dichloromethane, which was stirred under ice cooling. At a temperature below 20° C., 65 g (0.6 mole) of trimethylsilyl chloride was added dropwise to the solution, which was aged for 30 minutes at the temperature. Then, a Grignard reagent which had been prepared from 14.6 g (0.6 mole) of metallic magnesium, 67.5 g (0.6 mole) of chlorobenzene and 168 g of tetrahydrofuran (THF) was added dropwise at a temperature below 20° C. The reaction solution was aged for one hour, after which 50 g of water at a temperature below 20° C. was added to quench the reaction. To this solution, 150 g of water, 10 g of 12N hydrochloric acid, and 200 g of diethyl ether were further added. The water layer was separated and washed with 100 g of diethyl ether, yielding an aqueous solution of triphenylsulfonium chloride. The compound in aqueous solution form was used in the subsequent reaction without further isolation.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08048610B2uspto-grants-2011_11