Acetonitrile → HCID 583430, Verbindung

HRID 1518596Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1518596
[C:1](#[N:3])[CH3:2].C([Li])CCC.Br[C:10]1[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][N:11]=1>C1COCC1>[CH3:16][C:13]1[CH:14]=[CH:15][C:10]([CH2:2][C:1]#[N:3])=[N:11][CH:12]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
78 °C

Versuchsvorschrift

To a solution of anhydrous acetonitrile (10.1 mL, 191.83 mmol, 3.3 equiv.) in dry THF (500 mL) was added dropwise n-butyl lithium (2.5 M in hexane, 69.8 mL, 174.39 mmol, 3 equiv.) at minus 78° C. under a nitrogen atmosphere. The resulting white suspension was stirred at minus 78° C. for 1 hour, and then a solution of 2-bromo-5-methylpyridine (10.0 g, 58.13 mmol, 1 equiv.) in dry THF (30 mL) was added. The reaction mixture was kept at minus 78° C. for 1 hour and then warmed up slowly to room temperature and stirred for another hour. Ice/water was added and the layer was separated. The organic layer was washed with water and brine, dried over MgSO4, filtered, and evaporated to give 18 g of crude product, which was used for next step reaction without further purification.

Aufarbeitung

  1. waitThe reaction mixture was kept at minus 78° C. for 1 hour
  2. temperaturewarmed up slowly to room temperature
  3. stirringstirred for another hour
  4. customthe layer was separated
  5. washThe organic layer was washed with water and brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-6f390e37b14a4008b2a673f8b0fed084
Quelldatensatz
uspto-grants-2015_07
Patentnummer
US09072313B2

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