Reaktion #1807063

ord-9bd898fb93e34e8e8f45cdbfc1350a82

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent is removed
  2. 2
    workup.ADDITIONthe aqueous residue is diluted with the solution of base, preferably saturated sodium carbonate
  3. 3
    Extraktionthe product is extracted to organic halogenated solvent, preferably dichloromethane

Vorschrift

2-[phenethyl]-5-[(3,4-methylenedioxy)benzoyl]pyrrolidine trifluoroacetate (XIV) is reduced with metal borohydride, preferably with sodium borohydride, in a lower alcohol, preferably ethanol or methanol, at -10° to +20° C. The solvent is removed, the aqueous residue is diluted with the solution of base, preferably saturated sodium carbonate, and the product is extracted to organic halogenated solvent, preferably dichloromethane, to result in ±trans erythro 2-[phenethyl]-5-[(3,4-methylenedioxy)-α-hydroxybenzyl]pyrrolidine compound (XV). ##STR16##

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04543361uspto-grants-1985_09