反应详情

温度

50 °C

A stirred solution of 12.3 grams (0.051 mole) of 7-amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuran and 30 mL of toluene in 200 mL of ethanol is cooled in an ice-bath, and 5.6 mL (0.102 mole) of concentrated sulfuric acid is added slowly, followed by 5.6 grams (0.082 mole) of sodium nitrite. Upon completion of addition, the ice-bath is removed, and the reaction mixture is warmed to 50° C. The reaction mixture temperature is then brought to about 75° C., where it is stirred for 30 minutes. After this time the reaction mixture is heated at reflux for one hour and then is poured into 200 mL of water. The mixture is extracted with two 150 mL portions of diethyl ether. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residual oil. The oil is subjected to column chromatography on silica gel. Elution is accomplished using petroleum ether. The product-containing fractions are combined and concentrated under reduced pressure, yielding 3.6 grams of 4-bromo-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum is consistent with the proposed structure.

1. additionUpon completion of addition
2. customthe ice-bath is removed
3. customis then brought to about 75° C.
4. temperatureAfter this time the reaction mixture is heated
5. temperatureat reflux for one hour
6. additionis poured into 200 mL of water
7. extractionThe mixture is extracted with two 150 mL portions of diethyl ether
8. dry with materialThe combined extracts are dried with magnesium sulfate
9. filtrationfiltered
10. concentrationThe filtrate is concentrated under reduced pressure to a residual oil
11. washElution
12. concentrationconcentrated under reduced pressure