Reacción #1339655

ord-15a807b446cc4db7aef5b1021bde1dc3

Disolventes

Condiciones de reacción

Temperatura
20°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONafter complete addition the solution
  2. 2
    Extracciónextracted with diethyl ether (2×100 ml)
  3. 3
    LavadoThe ethereal extracts were washed with water
  4. 4
    Secadodried over anhydrous sodium sulphate
  5. 5
    Otrothe solvent removed

Procedimiento

cis-2,6-Dimethylmorpholine (8.9 g, 0.077 mol) was added dropwise to a solution of 2-(5-t-butylfuran-2-yl)-cyclopropanecarbonyl chloride (3.5 g, 0.0154 mol) in sodium dried ether (40 ml) at 10° C. and after complete addition the solution was stirred at 20° C. for 3 hours. The reaction mixture was poured into water and extracted with diethyl ether (2×100 ml). The ethereal extracts were washed with water, dried over anhydrous sodium sulphate, and the solvent removed to give 2-(5-t-butylfuran-2-yl)-cyclopropanecarbonyl-2,6-cis-dimethylmorpholine as a yellow oil. This oil was separated by column chromatography [silica eluted with petroleum ether ethyl acetate (1:1)] to give 2-(5-t-butylfuran-2-yl)-trans-cyclopropanecarbonyl-2,6-cis-dimethylmorpholine (1.43 g, 30%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04743602uspto-grants-1988_05