Reacción #684971

ord-61e35bb18f3f4c16ac066b8c62c662e6

Ecuación de reacción

O=C(O)C(F)(F)F
Trifluoroacetic acid
CCCCc1ccc(Cc2ncccc2OCOC)cc1
compound
CCCCc1ccc(Cc2ncccc2OCOC)cc1
2-(4-Butylbenzyl)-3-(methoxymethoxy)pyridine
O=C([O-])O.[Na+]
sodium hydrogencarbonate
CCOC(C)=O
ethyl acetate
CCCCc1ccc(Cc2ncccc2O)cc1
title compound
Rendimiento 88.8%
CCCCc1ccc(Cc2ncccc2O)cc1
2-(4-Butylbenzyl)-3-pyridinol
Rendimiento 88.8%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadothe reaction mixture was washed with saturated brine
  2. 2
    Concentraciónconcentrated under reduced pressure
  3. 3
    OtroThe residue was purified by silica gel column chromatography

Procedimiento

Trifluoroacetic acid (1 ml) was added to a solution of the compound of Example B229 (256 mg, 0.849 mmol) in methylene chloride (5 ml), and this reaction mixture was stirred at room temperature overnight. After a saturated aqueous sodium hydrogencarbonate solution and ethyl acetate were added, the reaction mixture was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (182 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07897387B2uspto-grants-2011_03