Reacción #56668

ord-f153600557c0416791bf202cd4833cdf

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with ethyl acetate
  2. 2
    Otrodried
  3. 3
    Otrothe solvent is evaporated off
  4. 4
    OtroThe residue is purified by chromatography on a silica gel column
  5. 5
    Lavadoeluting with an 8/2 cyclohexane/ethyl acetate mixture
  6. 6
    OtroThe compound of the title is obtained

Procedimiento

A mixture of 2.0 g (0.0008 mol) of trans-ethyl 4-(4-aminocyclohexyl)benzoate, 1.25 ml of triethylamine and 1.26 ml (0.0084 mol) of benzyl chloroformate at 95% in 40 ml of dimethylformamide is stirred at room temperature for 3 hours. The mixture is poured into water, extracted with ethyl acetate and dried, and the solvent is evaporated off. The residue is purified by chromatography on a silica gel column, eluting with an 8/2 cyclohexane/ethyl acetate mixture. The compound of the title is obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07419974B2uspto-grants-2008_09