Reacción #324053

ord-92964299de394349bb5b29b1a5822017

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe mixture is then filtered
  2. 2
    OtroThe filtrate is subsequently evaporated to dryness under vacuum
  3. 3
    OtroThis gives an oily residue
  4. 4
    Otroresults in the formation of a precipitate, which
  5. 5
    Filtraciónis filtered off
  6. 6
    Otro[The crystalline product thus obtained
  7. 7
    Otrois recrystallized

Procedimiento

0.7 g cis-2-methyl-3,3a,8,12b-tetrahydro-dibenzo [1,2;5,6]cyclohepta[3,4-c]pyrrol-1(2H)-one is dissolved in 25 ml dry ether/tetrahydrofuran (1:1). This solution is slowly added at 0° C. to a suspension of 0.35 g LiAlH4 in 20 ml ether/t.h.f. (1:1). After stirring for 15 minutes, water is added and the mixture is then filtered. The filtrate is subsequently evaporated to dryness under vacuum. This gives an oily residue, weighing about 0.7 g. Addition of 8 ml ethanol to this residue results in the formation of a precipitate, which is filtered off. [The crystalline product thus obtained is recrystallized, giving 0.25 g 2-methyl-2,3,3a,8-tetrahydro-dibenzo [1,2;5,6]cyclohepta[3,4-c]pyrrole of melting point 128°-131° C. (=enamine according to formula III)].

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04158058uspto-grants-1979_06