반응 #302855

ord-e15c1c71cd694b0190755e567dcdb3df

반응 방정식

BrB(Br)Br
boron tribromide
COc1ccc(-c2cc(=O)c3cc(Br)ccc3o2)cc1
compound 15
COc1ccc(-c2cc(=O)c3cc(Br)ccc3o2)cc1
6-bromo-4′-methoxyflavone
O=c1cc(-c2ccc(O)cc2)oc2ccc(Br)cc12
compound 16
O=c1cc(-c2ccc(O)cc2)oc2ccc(Br)cc12
6-bromo-4′-hydroxyflavone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도under cooling on ice
  2. 2
    기타the obtained mixture was then reacted
  3. 3
    기타After completion of the reaction
  4. 4
    기타purified water (100 ml)
  5. 5
    workup.ADDITIONwas added to the reaction solution
  6. 6
    추출the dichloromethane layer was extracted
  7. 7
    건조The extract was dried over anhydrous sodium sulfate
  8. 8
    workup.DISTILLATIONthe solvent was then distilled away under reduced pressure

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08192717B2uspto-grants-2012_06