Reacción #4509

ord-af833aac68e84efd9b9b7fe09d4bd9be

Disolventes

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe precipitate filtered off
  2. 2
    Otrosolvent removed from the filtrate under reduced pressure
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in 5 ml of tetrahydrofuran and to this solution
  4. 4
    workup.ADDITIONwas added dropwise a solution of ammonia in tetrahydrofuran until the reaction
  5. 5
    workup.ADDITIONThe mixture was poured into water
  6. 6
    Extracciónextracted with ethyl acetate
  7. 7
    SecadoThe organic solution was dried over magnesium sulfate
  8. 8
    Otroevaporated to an oil which
  9. 9
    Otrowas chromatographed on silica gel
  10. 10
    Lavadoeluting with a 1:1 mixture of ethyl acetate and hexane
  11. 11
    workup.STIRRINGThe purified product was stirred with a mixture of ether and hexane
  12. 12
    Filtraciónfiltered

Procedimiento

To a solution of 500 mgs of ethyl (E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-thiohexenoate in 10 ml of benzene cooled in an ice bath was added 0.1 ml of pyridine and 6 ml of a 12.5% solution of phosgene in benzene. The solution was stirred at 25° C. overnight, the precipitate filtered off and solvent removed from the filtrate under reduced pressure. The residue was dissolved in 5 ml of tetrahydrofuran and to this solution was added dropwise a solution of ammonia in tetrahydrofuran until the reaction was complete. The mixture was poured into water and extracted with ethyl acetate. The organic solution was dried over magnesium sulfate and evaporated to an oil which was chromatographed on silica gel, eluting with a 1:1 mixture of ethyl acetate and hexane. The purified product was stirred with a mixture of ether and hexane and filtered giving ethyl (E)-6-(1,3-dihydro-4-carbamoyl oxy-6-methoxy-7-methyl-3-oxo-5-iso benzofuranyl)-4-methyl-4-thiohexenoate, mp 145°-147° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04725622uspto-grants-1988_02