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Thionyl Chloride → 2,4-Dimethylpyridin-3-amine

HRID 383703
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 383703
[CH3:1][C:2]1[N:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1C(O)=O.S(Cl)(Cl)=O.[N-:16]=[N+]=[N-].[Na+]>O>[CH3:1][C:2]1[C:3]([NH2:16])=[C:7]([CH3:11])[CH:8]=[CH:9][N:10]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 24386Thionyl ChlorideHCID 33557Sodium AzideHCID 15125612,4-Dimethyl-3-pyridinecarboxylic acid

Produkt 1

HCID 149107812,4-Dimethylpyridin-3-amineAusbeute 74 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C
Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Versuchsvorschrift

A mixture of 1a (0.98 g, 6.5 mmol) and thionyl chloride (5 ml) was heated to 60° C. for 1 hour. The mixture was concentrated to dryness. The mixture was then dissolved in acetone (10 ml) prior to the addition of NaN3 (0.65 g, 10 mmol) and water (5 ml). The solution was heated to 70° C. for 1 hour. Acetone was evaporated from the reaction mixture which was washed with brine and extracted with ethyl acetate. The organic layer was dried over MgSO4, concentrated and chromatographed to yield 1b (0.585 g, 4.79 mmol, 74%).

Aufarbeitung

  1. concentrationThe mixture was concentrated to dryness
  2. dissolutionThe mixture was then dissolved in acetone (10 ml)
  3. temperatureThe solution was heated to 70° C. for 1 hour
  4. customAcetone was evaporated from the reaction mixture which
  5. washwas washed with brine
  6. extractionextracted with ethyl acetate
  7. dry with materialThe organic layer was dried over MgSO4
  8. concentrationconcentrated
  9. customchromatographed

Quellen und Nachweise

ORD-Eintrag
ord-161e9a64b288476da7e8ad850f7924be
Quelldatensatz
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08367684B2

Notizen zur Reaktion

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