反応 #1135824

ord-f7ec29ed07a948a299aa2cc576b14f56

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was refluxed
  2. 2
    その他on a rotary evaporator
  3. 3
    workup.ADDITIONpoured
  4. 4
    温度chilled
  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
    ろ過The pale pink solid was collected by suction filtration
  9. 9
    その他The solid was dried on the freeze dryer for 3 hours (8.31 g, 59%)

実験手順

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%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09381186B2uspto-grants-2016_07