Reacción #346449

ord-1f4109b6444941dcb8d0392730d445b1

Condiciones de reacción

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

Tratamiento posterior

  1. 1
    Otroformed by the addition of 50 mg
  2. 2
    OtroAfter approximately 4 hours the solvent is removed from the reaction mixture and 20 ml
  3. 3
    workup.ADDITIONof water is added to the residue
  4. 4
    ExtracciónThe resultant aqueous mixture is extracted with ether
  5. 5
    Lavadothe ether extracts washed with water
  6. 6
    Secadodried over magnesium sulfate
  7. 7
    Otroevaporated

Procedimiento

2,3-Epoxypropyl isopropyl ether (1.16 g.) in several ml. of dry tetrahydrofuran is added to a stirred suspension formed by the addition of 50 mg. of sodium hydride (56% dispersion in mineral oil) to 2.2 g. 8. of n-dodecylthiol in 50 ml. tetrahydrofuran. The mixture is then stirred at 60° C. After approximately 4 hours the solvent is removed from the reaction mixture and 20 ml. of water is added to the residue. The resultant aqueous mixture is extracted with ether and the ether extracts washed with water, dried over magnesium sulfate and evaporated to yield 1-(n-dodecylthio)-3-isopropoxy-2-propanol.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04036974uspto-grants-1977_07