Reaction #1135824
ord-f7ec29ed07a948a299aa2cc576b14f56
Reaction equation
Acetic acid 3-(4-hydroxy-phenyl)-8-methyl-4-oxo-chroman-7-yl ester
imidazole
→
7-Hydroxy-3-(4-hydroxy-phenyl)-8-methyl-chroman-4-one
Reagents
None
Solvents
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1TemperatureThe reaction mixture was refluxed
- 2Otheron a rotary evaporator
- 3workup.ADDITIONpoured
- 4Temperaturechilled
- 5workup.DISTILLATIONdistilled water (1.9 L)
- 6workup.WAITThe water crash out was left
- 7workup.STIRRINGstirring in the cold room overnight
- 8FiltrationThe pale pink solid was collected by suction filtration
- 9OtherThe 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%).