Resorcinol → 1-(2,4-Dihydroxyphenyl)-2-methylpropan-1-one
Reaktionsgleichung
[C:1]1([CH:8]=[CH:7][CH:6]=[C:4]([OH:5])[CH:3]=1)[OH:2].[C:9](O)(=[O:13])[CH:10]([CH3:12])[CH3:11].B(F)(F)F>CC([O-])=O.[Na+]>[OH:2][C:1]1[CH:3]=[C:4]([OH:5])[CH:6]=[CH:7][C:8]=1[C:9](=[O:13])[CH:10]([CH3:12])[CH3:11]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Resorcinol (10.0 g, 91 mmol) and isobutyric acid (8.00 g, 1 eq.) were treated with BF3-etherate (68 mL, 6 eq.) and heated for 1.5 h to 90° C. After cooling the reaction mixture was carefully poured onto 500 mL of 10% aq. NaOAc solution, twofold extracted with AcOEt, washed with water, dried over sodium sulfate, and evaporated to dryness to leave 18.5 g of the title compound as light brown oil.
Aufarbeitung
- temperatureheated for 1.5 h to 90° C
- temperatureAfter cooling the reaction mixture
- extractiontwofold extracted with AcOEt
- washwashed with water
- dry with materialdried over sodium sulfate
- customevaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-a94e8e7cdcdd4d02a09c677b9870aca8
- Quelldatensatz
- uspto-grants-2009_05
- Patentnummer
- US07534788B2
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