Reacción #302855

Ecuación de reacción

boron tribromide

compound 15

6-bromo-4′-methoxyflavone

→

compound 16

6-bromo-4′-hydroxyflavone

Disolventes

dichloromethane

dichloromethane

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaunder cooling on ice
2. 2
   Otrothe obtained mixture was then reacted
3. 3
   OtroAfter completion of the reaction
4. 4
   Otropurified water (100 ml)
5. 5
   workup.ADDITIONwas added to the reaction solution
6. 6
   Extracciónthe dichloromethane layer was extracted
7. 7
   SecadoThe extract was dried over anhydrous sodium sulfate
8. 8
   workup.DISTILLATIONthe solvent was then distilled away under reduced pressure

Procedimiento

A dichloromethane solution (12 ml) that contained boron tribromide was slowly added to a dichloromethane solution (215 ml) that contained compound 15 (400 mg, 1.21 mmol) while stirring under cooling on ice, and the obtained mixture was then reacted. After completion of the reaction, purified water (100 ml) was added to the reaction solution, and the dichloromethane layer was extracted. The extract was dried over anhydrous sodium sulfate, and the solvent was then distilled away under reduced pressure. The residue was subjected to silica gel column chromatography using ethyl acetate/hexane (2/5) as an elution solvent, so as to obtain a product of interest, 6-bromo-4′-hydroxyflavone (compound 16). Yield: 50 mg (yield constant: 13.1%) 1H NMR (300 MHz, CDCl3) δ10.38 (s, 1H), 8.09 (s, 1H), 7.97-8.00 (m, 3H), 7.76 (d, J=9.0 Hz, 1H), 6.93-6.96 (m, 3H).

Fuente