Reacción #1994312

ord-511aac09fa314a5f967c78ef6433e16c

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITION) was added drop wise to the solution
  2. 2
    LavadoThe reaction mixture was washed twice with saturated sodium bicarbonate solution and once with brine
  3. 3
    SecadoThe organic phase was then dried with anhydrous magnesium sulfate
  4. 4
    OtroThe solvent was removed with a rotary evaporator
  5. 5
    workup.DISTILLATIONthe crude product was distilled under vacuum

Procedimiento

A solution of 3-mercapto-1-butanol (106 g, 1 mol, synthesized as above) and PTSA (paratoluenesulfonic acid monohydrate, 38 g, 0.2 mol, commercially available from Sigma-Aldrich, Inc.) in 400 mL of CH2Cl2 (dichloromethane) were cooled with an ice bath. Butyraldehyde (106 mL, 1.2 mol, commercially available from Sigma-Aldrich, Inc.) was added drop wise to the solution, and the reaction mixture was stirred with cooling for half an hour and at room temperature for another 1 hour. The reaction mixture was washed twice with saturated sodium bicarbonate solution and once with brine. The organic phase was then dried with anhydrous magnesium sulfate. The solvent was removed with a rotary evaporator and the crude product was distilled under vacuum to provide 2-ethyl-4-methyl-1,3-oxathiane (98 g), which had a boiling point of 80° C. at a pressure of 10.4 mmHg.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08598110B2uspto-grants-2013_12