Reaktion #302856

ord-003cbe4ae842490aabef50107c94554a

Reaktionsgleichung

BrB(Br)Br
boron tribromide
COc1ccc(-c2cc(=O)c3cc(I)ccc3o2)cc1
compound 19
COc1ccc(-c2cc(=O)c3cc(I)ccc3o2)cc1
6-iodo-4′-methoxyflavone
O=c1cc(-c2ccc(O)cc2)oc2ccc(Br)cc12
compound 20
O=c1cc(-c2ccc(O)cc2)oc2ccc(Br)cc12
6-bromo-4′-hydroxyflavone

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder cooling on ice
  2. 2
    SonstigeAfter completion of the reaction
  3. 3
    Sonstigepurified water (80 ml)
  4. 4
    workup.ADDITIONwas added to the reaction solution
  5. 5
    Extraktionthe dichloromethane layer was extracted
  6. 6
    TrocknenThe extract was dried over anhydrous sodium sulfate
  7. 7
    workup.DISTILLATIONthe solvent was then distilled away under reduced pressure

Vorschrift

A dichloromethane solution (4.9 ml) that contained boron tribromide was slowly added to a dichloromethane solution (85 ml) that contained compound 19 (185 mg, 0.489 mmol) while stirring under cooling on ice, and the reaction was then carried out for 30 hours. After completion of the reaction, purified water (80 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 (1/4) as an elution solvent, so as to obtain a product of interest, 6-bromo-4′-hydroxyflavone (compound 20). Yield: 79 mg (yield constant: 44.3%) 1H NMR (300 MHz, DMSO6) 610.37 (s, 1H), 8.27 (s, 1H), 8.28-8.30 (m, 1H), 7.98 (d, J=8.4 Hz, 2H), 7.61 (d, J=8.7 Hz, 1H), 6.93-6.95 (m, 3H). MS m/z 364 (M+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08192717B2uspto-grants-2012_06