Reacción #50893
ord-91ba5b85156544099c3e46dc24f4ee38
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroA flask equipped with a stirrer
- 2Temperaturathe resulting mixture was cooled to −2° C
- 3Otroto terminate
- 4Otrothe reaction
- 5workup.STIRRINGstirred further
- 6FiltraciónThe reactant was filtered
- 7Lavadowashed with water
- 8Otrodried
- 9OtroThe resulting dry cake
- 10Lavadowas washed with ethanol
Procedimiento
A flask equipped with a stirrer and a thermometer was charged with 69.8 g of glacial acetic acid and 27.9 g of 3-bromodibenzothiophene-5-oxide prepared in Example 1-1 in a nitrogen atmosphere, and cooled to 10° C. 239.8 g of concentrated sulfuric acid was added dropwise, and the resulting mixture was cooled to −2° C. Then 72.0 g of 70 wt % nitric acid was added dropwise at −2 to 8° C., and the resulting mixture was stirred at or below 5° C. for 2 hours. The reaction mass was poured into 1200 g of ice water to terminate the reaction, and stirred further. The reactant was filtered, washed with water, and dried. The resulting dry cake was washed with ethanol to obtain 31.9 g of 3-bromo-7-nitrodibenzothiophene-5-oxide. The product was subjected to elemental analysis, the results of which are as follows: