Reaktion #4144
ord-50974b72a97646e5b2e5616160666f39
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONAt the end of addition the reaction mixture
- 2workup.STIRRINGwas stirred at room temperature for 2 hours
- 3Temperaturheated to 75°-78° C. for 16 hours
- 4SonstigeThe reaction mixture was partitioned between methylene chloride (300 ml) and water (250 ml)
- 5SonstigeThe aqueous phase was separated
- 6Extraktionextracted twice with methylene chloride (150 ml)
- 7WaschenThe combined organic solution was washed twice with water, twice with HCl (2N, 100 ml), brine (2×50 ml)
- 8Trocknendried over Na2SO4
- 9Einengenconcentrated to about 50 ml
- 10workup.ADDITIONEther (50 ml) was added
- 11SonstigeThe product was crystallized out
- 12workup.WAITupon standing overnight
- 13Sonstige(about 16 hours)
- 14SonstigeRecrystallization from methylene chloride and ether
Vorschrift
A slurry was prepared comprising 5-chloroindoline (15.3 gm, 0.1 mole), dimethylsulfoxide (DMSO) [50 ml] and sodium hydride (5.28 gm, 50% in oil, washed with hexane). The slurry was permitted to stir at room temperature for 1 hour. To this a solution of o-fluorobenzamide (15.2 gm, 1.1 eq.) in DMSO (20 ml) was added dropwise with the temperature between 17°-19° C. At the end of addition the reaction mixture was stirred at room temperature for 2 hours, then heated to 75°-78° C. for 16 hours. The reaction mixture was partitioned between methylene chloride (300 ml) and water (250 ml). The aqueous phase was separated and extracted twice with methylene chloride (150 ml). The combined organic solution was washed twice with water, twice with HCl (2N, 100 ml), brine (2×50 ml), dried over Na2SO4, concentrated to about 50 ml. Ether (50 ml) was added. The product was crystallized out upon standing overnight (about 16 hours). The yield was 14.2 gm (52%); m.p. 137°-138° C. Recrystallization from methylene chloride and ether yielded 2-(5-chloro-indolin-1-yl)benzamide (11.82 gm) m.p. 137°-138° C.