Reacción #1736796

ord-609fd9f7f9b44d21b16d5886cfc09c4b

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder reflux
  2. 2
    ExtracciónThe mixture was then extracted three times with 50 ml
  3. 3
    Lavadowashed with aqueous sodium chloride solution
  4. 4
    Secadodried over magnesium sulfate
  5. 5
    FiltraciónThe solution was then filtered
  6. 6
    Otrohydrogen chloride gas was bubbled through it
  7. 7
    OtroSolvent was then removed under vacuum
  8. 8
    Otroleaving a gray oil, which
  9. 9
    Otrowas triturated with denatured alcohol
  10. 10
    Otroto obtain white crystals, which
  11. 11
    Lavadowere washed with diethyl ether
  12. 12
    Otrorecrystallized from dichloromethane/ethanol
  13. 13
    Otroto obtain 1.86 g

Procedimiento

A 2 g. portion of 6-hydroxy-2-(4-hydroxyphenyl)-3-[4-(2-piperidinoethoxy)benzoyl]benzo[b]-thiophene was suspended in 35 ml. of chloroform, and 3.5 g. of potassium carbonate was added. The flask was blanketed with nitrogen, and 2 mg. of 4-dimethylaminopyridine and 1.2 g. of benzoyl chloride were added. The mixture was heated in an 80° C. oil bath for 4 hours under reflux, and was then poured into a large amount of aqueous sodium chloride solution. The mixture was then extracted three times with 50 ml. portions of chloroform, and the organic layers were combined and washed with aqueous sodium chloride solution and dried over magnesium sulfate. The solution was then filtered, and hydrogen chloride gas was bubbled through it. Solvent was then removed under vacuum, leaving a gray oil, which was triturated with denatured alcohol and seeded with an authentic sample of the desired product to obtain white crystals, which were washed with diethyl ether and recrystallized from dichloromethane/ethanol to obtain 1.86 g. of the desired product, m.p. 235°-236° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04418068uspto-grants-1983_11