Reaktion #64749

ord-12b77248c78349309b3b268a58c4f4f8

Reaktionsbedingungen

Temperatur
5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONThe reaction is poured onto ice
  2. 2
    ExtraktionThe aqueous is extracted with methylene chloride
  3. 3
    Trocknendried over MgSO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated vacuo
  6. 6
    Sonstigeto afford a brown oil which
  7. 7
    Einengenconcentrated in vacuo
  8. 8
    Sonstigeto yield a white paste which

Vorschrift

The aniline of Example 51 (3.07 g, 17.95 mmol) is dissolved in 60 ml of glacial acetic acid and to this is added norcamphor 2.37 g, 21.54 mmol). The reaction is cooled to 5° C. and to it is added sodium, cyanoborohydride (1.36 g, 21.54 mmol). The reaction is poured onto ice and is pH adjusted to 7 with 1 normal NaOH solution. The aqueous is extracted with methylene chloride dried over MgSO4, filtered and concentrated vacuo to afford a brown oil which is flashed on SiO2 with ethyl acetate as the eluent. The appropriate fractions are combined and concentrated in vacuo to yield a white paste which is tritarted with ether to yield (0.57 g 10%) of the product as a white crystalline solid. MP=171°-174° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05414127uspto-grants-1995_05