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Formamide → 2-(5-Fluorobenzofur-7-yl)propionamide

HRID 1824960
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1824960
[F:1][C:2]1[CH:3]=[C:4]([CH:11]([CH3:17])[C:12](OCC)=[O:13])[C:5]2[O:9][CH:8]=[CH:7][C:6]=2[CH:10]=1.C([NH2:20])=O.C[O-].[Na+]>CN(C)C=O.C(OCC)(=O)C>[F:1][C:2]1[CH:3]=[C:4]([CH:11]([CH3:17])[C:12]([NH2:20])=[O:13])[C:5]2[O:9][CH:8]=[CH:7][C:6]=2[CH:10]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 713FormamideHCID 10942334Sodium MethoxideHCID 22144818HCID 22144818, Verbindung

Produkt 1

HCID 221448132-(5-Fluorobenzofur-7-yl)propionamideAusbeute 25 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittel
HCID 8857
Ethyl Acetate
Lösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a solution of 0.27 gm (1.15 mMol) ethyl 2-(5-fluorobenzofur-7-yl)propionate in 4 mL dimethylformamide were added sequentially 0.16 mL (3.91 mMol) freshly distilled formamide and 0.81 mL (0.80 mMol) sodium methoxide (1 M in methanol) dropwise and the resulting mixture was heated at 100° C. for 45 minutes. The reaction mixture was cooled to room temperature and was then diluted with 25 volumes of ethyl acetate. The mixture was then washed sequentially with water and saturated aqueous sodium chloride, and concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, eluting with 2:1 ethyl acetate:hexane. Fractions containing product were combined and concentrated under reduced pressure to provide 0.060 gm (25%) of the desired compound.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to room temperature
  2. washThe mixture was then washed sequentially with water and saturated aqueous sodium chloride
  3. concentrationconcentrated under reduced pressure
  4. washeluting with 2:1 ethyl acetate
  5. additionFractions containing product
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-813138b3309c42589e021090076a0b54
Quelldatensatz
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07045545B1

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