Reacción #6608

ord-8d935727faf84d70b9ee58a54f250c2e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder reflux for 3 h
  2. 2
    Temperaturacooled
  3. 3
    ExtracciónThe mixture was extracted three times with ether
  4. 4
    Lavadothe combined ether extracts were washed with water
  5. 5
    Secadodried over Na2SO4
  6. 6
    Concentraciónconcentrated

Procedimiento

A suspension of 3 g (9.4 mmol) of 4-cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether in 60 ml of ether was added dropwise under nitrogen to a suspension of 1 g (26 mmol) of lithium aluminum hydride in 50 ml of dry ether at 25° C. The mixture was then stirred under reflux for 3 h, cooled and hydrolyzed cautiously with water and sodium sulfate solution. The mixture was extracted three times with ether, and the combined ether extracts were washed with water, dried over Na2SO4 and concentrated. 3 g of the title compound of melting point 77°-79° C. remained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05248823uspto-grants-1993_09