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Ammonia → 3-Chloro-4,4-dimethylpent-2-enal

HRID 2408957
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2408957
P(Cl)(Cl)([Cl:3])=O.CN([CH:9]=[O:10])C.[CH3:11][C:12](=O)[C:13]([CH3:16])([CH3:15])[CH3:14].N>>[Cl:3][C:12]([C:13]([CH3:16])([CH3:15])[CH3:14])=[CH:11][CH:9]=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 222AmmoniaHCID 6228DimethylformamideHCID 6416PinacoloneHCID 24813Phosphorus oxychloride

Produkt 1

HCID 540583463-Chloro-4,4-dimethylpent-2-enalAusbeute 80 %

Versuchsvorschrift

Phosphorous oxychloride (18.77 mL, 200 mmol) was added dropwise to DMF (30.8 mL, 400 mmol) at 0-5° C. for 30 min. Pinacolone (10 g, 100 mmol) was added dropwise to the reaction mixture at the same temperature for 30 min. The mixture was allowed to rt and stirred for 2 h. The reaction mixture was poured into ice cold water and basified with ammonia solution. The solution was extracted with chloroform (3×200 mL) and the combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-EtoAc (97:3) as eluents to give the product as a pale green color oil (11.7 g, 80%).

Aufarbeitung

  1. customwas allowed to rt
  2. additionThe reaction mixture was poured into ice cold water
  3. extractionThe solution was extracted with chloroform (3×200 mL)
  4. washthe combined chloroform layer was washed with water, brine
  5. dry with materialdried over sodium sulfate
  6. filtrationThe solution was filtered
  7. customevaporated the solvent
  8. customThe residue was chromatographed over silica gel column

Quellen und Nachweise

ORD-Eintrag
ord-465de8153cb54704af761d8296558125
Quelldatensatz
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08815879B2

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