Ethanol → 5-(4-Methoxyphenyl)-2,2-dimethylfuran-3(2H)-one

HRID 1258262Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1258262
O[C:2]([CH3:16])([CH3:15])[C:3]#[C:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1)=[O:6].CC[OH:19]>>[CH3:14][O:13][C:10]1[CH:11]=[CH:12][C:7]([C:5]2[O:6][C:2]([CH3:16])([CH3:15])[C:3](=[O:19])[CH:4]=2)=[CH:8][CH:9]=1

Komponenten

3

Edukt 2

HCID 702Ethanol2×HCID 127225774-Hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-one

Produkt 1

HCID 145333195-(4-Methoxyphenyl)-2,2-dimethylfuran-3(2H)-oneAusbeute 92 %

Versuchsvorschrift

To a stirred solution of 4-hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-one (6 g, 0.027 mol) in ethanol (100 mL) diethyl amine (2.86 g, 0.027 mol) in EtOH (15 mL) was added dropwise at RT and the reaction mixture was stirred for additional 4 h. The EtOH was then removed and the mixture diluted with EtOAc (100 mL). The combined organic layers were washed with water (50 mL) and brine (20 mL), dried over Na2SO4, filtered and concentrated in vacuo to afford 5-(4-methoxyphenyl)-2,2-dimethylfuran-3(2H)-one (5.5 g, 92%).

Aufarbeitung

  1. customThe EtOH was then removed
  2. additionthe mixture diluted with EtOAc (100 mL)
  3. washThe combined organic layers were washed with water (50 mL) and brine (20 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ddf52f3a9f6a4d40a40190126d6c82ab
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08466148B2

Notizen zur Reaktion

Wird geladen…