Reaktion #64018

ord-df12137694794b8fbee01f301f5614e3

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeDerivative 3 (R=4-OCH3, n=7) is prepared by a procedure similar to
  2. 2
    workup.ADDITIONThe resulting diastereomeric mixture of cis- and trans-derivative 3 (R=4-OCH3, n=7)
  3. 3
    Sonstigeis flash-chromatographed on neutral silica gel

Vorschrift

Derivative 3 (R=4-OCH3, n=7) is prepared by a procedure similar to that described in Example 1 by reacting 1-(4-methoxyphenyl)-N-methyl-2-(1H-1,2,4-triazol-1-yl)ethanimine N-oxide (1: R=4-OCH3) with 1-decene (2: n=7). The resulting diastereomeric mixture of cis- and trans-derivative 3 (R=4-OCH3, n=7) is flash-chromatographed on neutral silica gel using chloroform-methanol (99:1 by volume) as eluent. Isomer A has a melting point of 89°-91° C. (ethyl acetate).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04767866uspto-grants-1988_08