Reacción #302854

ord-54020c6efa304eb485750fadda8bc881

Ecuación de reacción

COc1ccc(C(=O)CC(=O)c2cc(Br)ccc2O)cc1
compound 14
COc1ccc(C(=O)CC(=O)c2cc(Br)ccc2O)cc1
1-(5-bromo-2-hydroxyphenyl)-3-(4-methoxyphenyl)propan-1,3-dione
O=S(=O)(O)O
sulfuric acid
COc1ccc(-c2cc(=O)c3cc(Br)ccc3o2)cc1
compound 15
COc1ccc(-c2cc(=O)c3cc(Br)ccc3o2)cc1
6-bromo-4′-methoxyflavone

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturato reflux for 1 hour
  3. 3
    Otrowas returned to room temperature
  4. 4
    workup.ADDITIONice pieces were then added to the reaction solution
  5. 5
    FiltraciónThe precipitated crystal was collected by filtration

Procedimiento

A mixed solution consisting of compound 14 (2.67 g, 7.65 mmol), concentrated sulfuric acid (0.78 ml), and acetic acid (40 ml) was heated to reflux for 1 hour. The temperature of the resultant was returned to room temperature, and ice pieces were then added to the reaction solution. The precipitated crystal was collected by filtration, so as to obtain a product of interest, 6-bromo-4′-methoxyflavone (compound 15). Yield: 2.01 g (yield constant: 79.4%) 1H NMR (300 MHz, CDCl3) δ8.35 (s, 1H), 7.87 (d, J=9.0 Hz, 2H), 7.77 (d, J=9.0 Hz, 1H), 7.45 (d, J=9.3 Hz, 1H), 7.03 (d, J=9.0 Hz, 2H), 6.75 (s, 1H), 3.90 (s, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08192717B2uspto-grants-2012_06