Reacción #165929

ord-ebbc25a263864c7ebfdd52970f939874

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroreaction
  2. 2
    OtroReaction mass
  3. 3
    Filtraciónwas filtered through hyflow
  4. 4
    Concentraciónconcentrated to residue
  5. 5
    Filtraciónfiltered
  6. 6
    Otroto remove triethylamine HBr salt
  7. 7
    ConcentraciónFiltrate was concentrated

Procedimiento

Ethyl-2-(3-bromo-2-methoxytetrahydrofuran-3-yl)-2-oxoacetate (8.5 g) was dissolved in Ethanol (85 ml). Triethyl amine (3.66 g) was added to the reaction mass. 5% Palladium on Carbon (0.85 g) was added and reaction was hydrogenated at 4-5 kg pressure of Hydrogen for 8 hrs. Reaction mass was filtered through hyflow and concentrated to residue. This residue was slurried in methyltert-butylether (42 ml) and filtered to remove triethylamine HBr salt. Filtrate was concentrated to get oily residue of Ethyl-2-(2-methoxytetrahydrofuran-3-yl)-2-oxoacetate (yield 6.0 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08841467B2uspto-grants-2014_09