반응 #302856

ord-003cbe4ae842490aabef50107c94554a

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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+).

출처

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