Reaktion #163496

Reaktionsgleichung

2,6-Dibromo-4,8-dimethoxy-benzo[1,2-b:4,5-b′]dithiophene

boron tribromide

→

2,6-Dibromo-benzo[1,2-b:4,5-b′]dithiophene-4,8-diol

Lösungsmittel

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigedry/ice acetone bath with an ice/water bath
2. 2
   workup.WAITThe reaction mixture was left
3. 3
   Temperaturto warm to room temperature
4. 4
   workup.STIRRINGwhile stirring for 16 hours
5. 5
   Temperaturbefore cooling to 0° C
6. 6
   workup.ADDITIONWater (dropwise at first, 150 mL total) and additional dichloromethane (50 mL) were added
7. 7
   SonstigeThe dichloromethane was removed on the rotary evaporator
8. 8
   Filtrationthe solid was collected by filtration
9. 9
   WaschenThe solid was washed with water (25 mL) and dichloromethane (25 ml)
10. 10
    Sonstigeto give a pale blue/green crude solid
11. 11
    Sonstigeto be dried under vacuum
12. 12
    Sonstigeused in the next step without additional purification (287 mg)

Vorschrift

2,6-Dibromo-4,8-dimethoxy-benzo[1,2-b:4,5-b′]dithiophene (500 mg, 1.22 mmol., 1.00 equiv.) and dichloromethane (12 mL) were added to a 50 mL schlenk flask. The mixture was cooled to −78° C. and boron tribromide was added (1.0 M solution in dichloromethane, 2.5 mL, 2.5 mmol., 2.1 equiv.) slowly. The mixture was stirred for 15 minutes at −78° C. before replacing the dry/ice acetone bath with an ice/water bath. The reaction mixture was left to warm to room temperature while stirring for 16 hours before cooling to 0° C. Water (dropwise at first, 150 mL total) and additional dichloromethane (50 mL) were added. The dichloromethane was removed on the rotary evaporator and the solid was collected by filtration. The solid was washed with water (25 mL) and dichloromethane (25 ml) to give a pale blue/green crude solid to be dried under vacuum and used in the next step without additional purification (287 mg). 1H NMR (400 MHz, CDCl3) δ 10.13 (s, 2H), 7.71 (s, 2H).

Quelle