Reaktion #62083

Reaktionsgleichung

5-bromo-2-nitro-thioxanthen-9-one

borane THF

→

title compound

Ausbeute 100.0%

5-Bromo-2-nitro-9H-thioxanthene

Ausbeute 100.0%

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturTo a cooled
2. 2
   TemperaturThe reaction mixture was cooled (0° C.)
3. 3
   Sonstigethe excess borane was quenched with acetone
4. 4
   SonstigeThe solvent was evaporated in vacuo
5. 5
   Sonstigethe residue was triturated in saturated sodium bicarbonate (100 ml)
6. 6
   FiltrationThe solid was filtered
7. 7
   Waschenwashed with water
8. 8
   Sonstigedried overnight in a vacuum dissicator

Vorschrift

To a cooled (0° C.) suspension of 5-bromo-2-nitro-thioxanthen-9-one (23.03 g, 68.5 mmol) in anhydrous tetrahydrofuran (100 ml) under nitrogen atmosphere, was added drop wise borane-THF complex (151 ml, 1.0M in THF). The mixture was allowed to warm to room temperature with stirring overnight. The reaction mixture was cooled (0° C.) and the excess borane was quenched with acetone. The solvent was evaporated in vacuo and the residue was triturated in saturated sodium bicarbonate (100 ml). The solid was filtered, washed with water and dried overnight in a vacuum dissicator to give the title compound (22.07 g, 100%). 1HNMR (300 MHz, CDCl3): δH=4.02 (2H, s), 7.17 (1H, m), 7.27 (1H, m), 7.51 (1H, m), 7.62 (1H, m), 8.09 (1H, m), 8.20 (1H, d).

Quelle