Reaktion #807945
ord-7b245a96f12748eca039d7bf64d0b666
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeA flask equipped with a stirrer
- 2Sonstigepreheated to 80° C.
- 3workup.STIRRINGstirred at 80 to 85° C. for 5 hours
- 4Temperaturcooled to room temperature
- 5FiltrationThe reactant was filtered
- 6Extraktionextracted six times with 300 ml of ethyl acetate, and vacuum
- 7Einengenconcentrated
- 8SonstigeThe concentrate was purified by silica gel chromatography
Vorschrift
A flask equipped with a stirrer and a thermometer was charged with 209.3 g of concentrated sulfuric acid and 8.93 g of NaNO2 in a nitrogen atmosphere, and cooled to 2° C. Then 24.0 g of the intermediate 7-bromodibenzothiophene-3-yl-amine prepared in Example 1-3 was added, and stirred at 2 to 4° C. for 3 hours. The resulting mixture together with 99.8 g of water was poured into 348.7 g of 65 wt % sulfuric acid preheated to 80° C., stirred at 80 to 85° C. for 5 hours, and cooled to room temperature. The reactant was filtered, extracted six times with 300 ml of ethyl acetate, and vacuum concentrated. The concentrate was purified by silica gel chromatography using chloroform as an eluting solvent to obtain 7.11 g of objective 7-bromodibenzothiophene-3-ol. The 1H-NMR spectrum data and the results of elemental analysis of the product are shown below: