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Sodium Cyanide → Ethyl 4-(3-cyanopropyl)-4-cyano-1-piperidinecarboxylate

HRID 1274451
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1274451
Cl[CH2:2][CH2:3][CH2:4][C:5]1([C:16]#[N:17])[CH2:10][CH2:9][N:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:7][CH2:6]1.[C-:18]#[N:19].[Na+]>CN(C)C=O.O>[C:18]([CH2:2][CH2:3][CH2:4][C:5]1([C:16]#[N:17])[CH2:10][CH2:9][N:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:7][CH2:6]1)#[N:19]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 8929Sodium CyanideHCID 9838044Ethyl 4-(3-chloropropyl)-4-cyano-1-piperidinecarboxylate

Produkt 1

HCID 10198845Ethyl 4-(3-cyanopropyl)-4-cyano-1-piperidinecarboxylateAusbeute 88,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

To a solution of ethyl 4-(3-chloropropyl)-4-cyano-1-piperidinecarboxylate (12.7 g) in dimethylformamide (250 ml) was added sodium cyanide (24 g) under nitrogen, with stirring. The mixture was warmed at 140° C. overnight and then cooled to ambient temperature, diluted with water and extracted with ethyl acetate. The organic extracts were washed with saturated sodium chloride solution and water, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo. The residue was chromatographed, eluting with 2:1 heptane/ethyl acetate. The appropriate fractions were collected and concentrated to give 10.8 g (88.5%) of product. A portion was distilled to give the analytical sample, bp196-201° C. (4 mm of mercury).

Aufarbeitung

  1. temperaturecooled to ambient temperature
  2. extractionextracted with ethyl acetate
  3. washThe organic extracts were washed with saturated sodium chloride solution and water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated in vacuo
  7. customThe residue was chromatographed
  8. washeluting with 2:1 heptane/ethyl acetate
  9. customThe appropriate fractions were collected
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-97163a05293e42c9bed6c44c4224c896
Quelldatensatz
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06156901

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