Reacción #1736796
ord-609fd9f7f9b44d21b16d5886cfc09c4b
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaunder reflux
- 2ExtracciónThe mixture was then extracted three times with 50 ml
- 3Lavadowashed with aqueous sodium chloride solution
- 4Secadodried over magnesium sulfate
- 5FiltraciónThe solution was then filtered
- 6Otrohydrogen chloride gas was bubbled through it
- 7OtroSolvent was then removed under vacuum
- 8Otroleaving a gray oil, which
- 9Otrowas triturated with denatured alcohol
- 10Otroto obtain white crystals, which
- 11Lavadowere washed with diethyl ether
- 12Otrorecrystallized from dichloromethane/ethanol
- 13Otroto 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.