Reacción #335655

ord-adbb6ec7b9654d49bb9d1bf8fce374b3

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrorecooled to 0°-5° C.
  2. 2
    workup.WAITThe mixture was stored at room temperature overnight
  3. 3
    Otroall the solvents were removed
  4. 4
    ExtracciónThe residue was extracted with dichloromethane, water
  5. 5
    Lavadowashed
  6. 6
    Otrodried
  7. 7
    Filtraciónfiltered
  8. 8
    Otroevaporated
  9. 9
    OtroThis residue was purified by flash column chromatography
  10. 10
    Lavadoeluting with chloroform

Procedimiento

A 5 g portion of the above aldehyde was dissolved in a mixture of 100 ml of ethanol and 10 ml of dioxane. To this mixture, in an ice bath was added a solution of 1.61 g of ethylenediamine in ethanol. The mixture was stirred for one hour at room temperature, recooled to 0°-5° C. and 2.04 g of sodium borohydride added. The mixture was stored at room temperature overnight, water was added and all the solvents were removed. The residue was extracted with dichloromethane, water washed, dried, filtered and evaporated. This residue was purified by flash column chromatography, eluting with chloroform:-methanol (9:1), giving 2.39 g of 2-(3-methylbenzo[b]-thien-2-yl)piperazine.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05210193uspto-grants-1993_05