Reacción #95965

ord-1f9323f860a1473092bc4015766e1ed1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITION4,065,573, Example 41, part B) was added over 20 minutes
  2. 2
    FiltraciónThe inorganic gel in the mixture was filtered off
  3. 3
    OtroThe filtrate was dried by evaporation under vacuum

Procedimiento

A 0.4 g portion of lithium aluminum hydride (LAH) is cooled in 10 ml of diethyl ether under nitrogen atmosphere. Then 2.0 g of 8-cyano-[1,4-dioxaspiro[4.5]dec-8-yl]dimethylamine (U.S. Pat. No. 4,065,573, Example 41, part B) was added over 20 minutes while stirring at room temperature. Then, in turn, there was added 0.4 ml of water, 0.4 ml of 15 percent sodium hydroxide and 1.2 ml of water. The inorganic gel in the mixture was filtered off. The filtrate was dried by evaporation under vacuum. A thin layer chromatography (tlc) sample analysis showed the residue to be largely one spot material. The Nuclear Magnetic Resonance spectrum (NMR) for this material was very good for the above-named chemical intermediate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04346101uspto-grants-1982_08