Reacción #1049540

ord-1dd8ef94f2dd437fbdacdc1147908fb3

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónfiltered
  2. 2
    Concentraciónconcentrated
  3. 3
    OtroThe residue is chromatographed on 10 g of silica gel with hexane/ethyl acetate 19:1 (v/v)
  4. 4
    OtroRecrystallization of the product-containing fractions from ethanol

Procedimiento

A solution of 0.3 g of N,N'-dicyclohexyl-carbodiimide in 6 ml of dichloromethane is added dropwise at 0° C. within 15 minutes to a solution of 0.201 g of 4-(5-octyl-pyrimidin-2-yl)-benzoic acid, 0.116 g of cyclopentane-hexanol and 0.02 g of 4-dimethylaminopyridine in 10 ml of dichloromethane. The suspension is stirred at 0° C. for a further 1 hour, filtered and concentrated. The residue is chromatographed on 10 g of silica gel with hexane/ethyl acetate 19:1 (v/v). Recrystallization of the product-containing fractions from ethanol gives pure 6-cyclopentyl-hexyl 4-(5-octyl-pyrimidin-2-yl)-benzoate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05759443uspto-grants-1998_06