Reacción #1255226

ord-bf1a3af668ac4abbb310bc752e1b641b

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaby heating
  2. 2
    Temperaturaat reflux for 3 hours
  3. 3
    Lavadothe organic layer was washed with brine
  4. 4
    Secadodried (Na2CO4)
  5. 5
    Otroevaporated

Procedimiento

To a slurry of lithium aluminum deuteride (LiAlD4) (0.012 g) in anhydrous ether (1 mL) was added, with stirring, camphor (0.1 g) in ether (2 mL), followed by heating at reflux for 3 hours. After cooling to room temperature, the excess hydride was decomposed by addition of moist ether, then the organic layer was washed with brine, dried (Na2CO4) and evaporated to give a quantitative yield of deuteriated isoborneol (0.1 g). 2H NMR (hexanes): δ 3.75. See B. Belleau, J. Am. Chem. Soc., 82, p. 5751 (1960).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06620972B2uspto-grants-2003_09