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Isopropanol → HCID 45117314, Verbindung

HRID 2102905
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2102905
[CH3:1][C:2]([CH3:14])([CH3:13])[C:3]#[C:4][C:5]1[N:10]=[CH:9]C(C#N)=[CH:7][N:6]=1.[OH-:15].[K+].[CH:17]([OH:20])([CH3:19])C>O>[CH3:1][C:2]([CH3:14])([CH3:13])[C:3]#[C:4][C:5]1[N:10]=[CH:9][C:19]([C:17]([OH:20])=[O:15])=[CH:7][N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 3776IsopropanolHCID 14797Potassium HydroxideHCID 57804136HCID 57804136, Verbindung

Produkt 1

HCID 45117314HCID 45117314, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A mixture 2-(3,3-dimethylbut-1-ynyl)pyrimidine-5-carbonitrile (1.0 g, 0.005 mol) and potassium hydroxide (2.8 g, 0.05 mol) in isopropanol (40 mL) and water (10 mL) was heated at reflux for three hours. The mixture was allowed to cool to room temperature and concentrated under vacuum. Water (200 mL) was added and the mixture was cooled to 0° C., then conc. HCl was added until a pH of 6 was obtained. The resulting off-white precipitate was collected by filtration and washed with water to give the product as a solid. m/z=205 (M+1).

Aufarbeitung

  1. temperatureat reflux for three hours
  2. concentrationconcentrated under vacuum
  3. additionWater (200 mL) was added
  4. temperaturethe mixture was cooled to 0° C.
  5. additionconc. HCl was added until a pH of 6
  6. customwas obtained
  7. filtrationThe resulting off-white precipitate was collected by filtration
  8. washwashed with water

Quellen und Nachweise

ORD-Eintrag
ord-61ba0ab9033d45c8814379103ca02c56
Quelldatensatz
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07576099B2

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