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Toluene → 2-Methyl-1-(pyridin-3-yl)propan-1-one

HRID 1613644
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1613644
O1CCN(C([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)C#N)CC1.[OH-:16].[Na+].[CH:18](Br)([CH3:20])[CH3:19].[C:22]1(C)C=CC=CC=1>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[CH:18]([C:20]([C:10]1[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=1)=[O:16])([CH3:22])[CH3:19]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 1140TolueneHCID 63582-BromopropaneHCID 14798Sodium HydroxideHCID 303572Morpholin-4-yl(pyridin-3-yl)acetonitrile

Produkt 1

HCID 122813372-Methyl-1-(pyridin-3-yl)propan-1-one

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 67553
Tetrabutylammonium Iodide
Katalysator
HCID 962WaterLösungsmittel

Versuchsvorschrift

133 g (0.70 mol) of alpha-morpholino-3-pyridylacetonitrile, 25.7 g (0.07 mol) of tetrabutylammonium iodide, 278 g (3.5 mol) of 50% strength NaOH, 250 ml (2.65 mol) of isopropyl bromide and 300 ml of toluene, as a two-phase system, were heated at 50° C. for 4 hours with thorough mixing. Working up was carried out by adding water, separating the phases and washing the organic phase three times with water. After the solvent had been distilled off, the crude product in the form of an oil was added dropwise to half-concentrated H2SO4 at 60° C. After 2 hours, the mixture was brought to pH 9 with 50% strength NaOH and was extracted with toluene. The organic phase was washed three times with water and the wash solution was extracted 4 times with toluene. The collected toluene extracts were dried over Na2SO4 and filtered and the filtrate was evaporated down. The product was obtained as a dark oil.

Aufarbeitung

  1. customseparating the phases
  2. washwashing the organic phase three times with water
  3. distillationAfter the solvent had been distilled off
  4. additionthe crude product in the form of an oil was added dropwise to half-concentrated H2SO4 at 60° C
  5. extractionwas extracted with toluene
  6. washThe organic phase was washed three times with water
  7. extractionthe wash solution was extracted 4 times with toluene
  8. dry with materialThe collected toluene extracts were dried over Na2SO4
  9. filtrationfiltered
  10. customthe filtrate was evaporated down
  11. customThe product was obtained as a dark oil

Quellen und Nachweise

ORD-Eintrag
ord-8daa1337d82542628b20ed2a6baf94a4
Quelldatensatz
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05194441

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