Ethanol → 4-(5,5-Dimethyl-4-oxo-4,5-dihydrofuran-2-yl)benzonitrile

HRID 1425849Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1425849
O[C:2]([CH3:16])([CH3:15])[C:3]#[C:4][C:5]([C:7]1[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=1)=[O:6].C(NCC)C.C([OH:24])C>>[CH3:15][C:2]1([CH3:16])[O:6][C:5]([C:7]2[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=2)=[CH:4][C:3]1=[O:24]

Komponenten

4

Edukt 3

HCID 702Ethanol2×HCID 8021DiethylamineHCID 666439664-(4-Hydroxy-4-methylpent-2-ynoyl)benzonitrile

Produkt 1

HCID 595801574-(5,5-Dimethyl-4-oxo-4,5-dihydrofuran-2-yl)benzonitrile

Versuchsvorschrift

To a stirred solution of crude 4-(4-hydroxy-4-methylpent-2-ynoyl)benzonitrile (1.2 g, 5.60 mmol) in ethanol (12 mL), a solution of diethyl amine (0.58 mL, 5.60 mmol) in EtOH (5 mL) was added dropwise at RT. The reaction mixture was then stirred for additional 1 h. The ethanol was removed and the mixture then diluted with EtOAc (50 mL). The combined organic layers were washed with water (10 mL), brine (10 mL), dried over Na2SO4, filtered, and concentrated in vacuo to afford crude 4-(5,5-dimethyl-4-oxo-4,5-dihydrofuran-2-yl)benzonitrile (1.2 g) as a light green semi solid which was taken on to the next step without further purification.

Aufarbeitung

  1. customThe ethanol was removed
  2. additionthe mixture then diluted with EtOAc (50 mL)
  3. washThe combined organic layers were washed with water (10 mL), brine (10 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-fe6210a543c94f77886f197fae182ba4
Quelldatensatz
uspto-grants-2015_01
Patentnummer
US08933074B2

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