Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:12])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1.C1N2CN3CN(C2)CN1C3.FC(F)(F)[C:25](O)=[O:26]>>[CH3:1][O:2][C:3](=[O:12])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[C:7]([CH:25]=[O:26])[CH:6]=1Komponenten
4
Versuchsvorschrift
Methyl(4-hydroxyphenyl)acetate (1.66 g) is dissolved in trifluoroacetic acid (20 ml), thereto is added hexamethylenetetramine (700 mg) and the mixture is heated under reflux for 2 hours. The reaction solution is concentrated under reduced pressure, thereto is poured ice-water, and then the mixture is extracted with ethyl acetate. The organic layer is washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate and evaporated to remove the solvent under reduced pressure. The resulting residue is purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1 followed by 4/1) to give the title compound (1.08 g).
Aufarbeitung
- temperaturethe mixture is heated
- temperatureunder reflux for 2 hours
- concentrationThe reaction solution is concentrated under reduced pressure
- additionis poured ice-water
- extractionthe mixture is extracted with ethyl acetate
- washThe organic layer is washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine
- dry with materialdried over sodium sulfate
- customevaporated
- customto remove the solvent under reduced pressure
- customThe resulting residue is purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1 followed by 4/1)
Quellen und Nachweise
- ORD-Eintrag
- ord-f03f86434a1f4c6c989e07b0698a70bc
- Quelldatensatz
- uspto-grants-2009_05
- Patentnummer
- US07531537B2
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