Reacción #80927
ord-5eddf7418b044d549a8eb181a1c08fba
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas then added
- 2OtroThe ice bath was then removed
- 3TemperaturaAfter this time the reaction mixture was warmed to 95° C.
- 4workup.STIRRINGwhere it stirred for one hour
- 5TemperaturaThe reaction mixture was then cooled
- 6workup.ADDITIONpoured into 200 mL of water
- 7ExtracciónThe mixture was extracted with two 150 mL portions of diethyl ether
- 8SecadoThe combined extracts were dried with magnesium sulfate
- 9Filtraciónfiltered
- 10ConcentraciónThe filtrate was concentrated under reduced pressure to a residue
- 11LavadoElution
- 12Concentraciónconcentrated under reduced pressure
Procedimiento
A stirred solution of 5.1 grams (0.018 mole) of 7-amino-4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran and 25 mL of toluene in 100 mL of ethanol was cooled in an ice bath, and 2 mL (0.036 mole) of concentrated sulfuric acid was added slowly. Upon completion of addition, 2.0 grams (0.029 mole) of sodium nitrite was then added. The ice bath was then removed, and the reaction mixture was warmed to 75° C., where it stirred for 30 minutes. After this time the reaction mixture was warmed to 95° C., where it stirred for one hour. The reaction mixture was then cooled and poured into 200 mL of water. The mixture was extracted with two 150 mL portions of diethyl ether. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel. Elution was accomplished using petroleum ether. The product-containing fractions were combined and concentrated under reduced pressure, yielding 3.6 grams of 4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum was consistent with the proposed structure.