Reaction #1135824

ord-f7ec29ed07a948a299aa2cc576b14f56

Reaction equation

CC(=O)Oc1ccc2c(c1C)OCC(c1ccc(O)cc1)C2=O
Acetic acid 3-(4-hydroxy-phenyl)-8-methyl-4-oxo-chroman-7-yl ester
c1c[nH]cn1
imidazole
Cc1c(O)ccc2c1OCC(c1ccc(O)cc1)C2=O
7-Hydroxy-3-(4-hydroxy-phenyl)-8-methyl-chroman-4-one

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureThe reaction mixture was refluxed
  2. 2
    Otheron a rotary evaporator
  3. 3
    workup.ADDITIONpoured
  4. 4
    Temperaturechilled
  5. 5
    workup.DISTILLATIONdistilled water (1.9 L)
  6. 6
    workup.WAITThe water crash out was left
  7. 7
    workup.STIRRINGstirring in the cold room overnight
  8. 8
    FiltrationThe pale pink solid was collected by suction filtration
  9. 9
    OtherThe solid was dried on the freeze dryer for 3 hours (8.31 g, 59%)

Procedure

Acetic acid 3-(4-hydroxy-phenyl)-8-methyl-4-oxo-chroman-7-yl ester (18.37 g), imidazole (21.18 g, 6 equivalents) and 100% EtOH (536 ml) were added to a round bottom flask (2 L). The reaction mixture was refluxed and monitored by HPLC. The reaction was completed at 8 hours. The reaction mixture was reduced (˜130 ml) on a rotary evaporator and poured into stirred, chilled distilled water (1.9 L). The water crash out was left stirring in the cold room overnight. The pale pink solid was collected by suction filtration. 1H NMR of the solid indicated it was 7-Hydroxy-3-(4-hydroxy-phenyl)-8-methyl-chroman-4-one with >95% purity. The solid was dried on the freeze dryer for 3 hours (8.31 g, 59%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09381186B2uspto-grants-2016_07