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Dimethylformamide → 2-chloro-4,4-diMethylcyclohex-1-enecarbaldehyde

HRID 573128
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 573128
CN(C)[CH:3]=[O:4].P(Cl)(Cl)([Cl:8])=O.[CH3:11][C:12]1([CH3:19])[CH2:17][CH2:16][CH2:15][C:14](=O)[CH2:13]1>ClCCl>[Cl:8][C:14]1[CH2:13][C:12]([CH3:19])([CH3:11])[CH2:17][CH2:16][C:15]=1[CH:3]=[O:4]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 76322Cyclohexanone, 3,3-dimethyl-

Produkt 1

HCID 866428722-chloro-4,4-diMethylcyclohex-1-enecarbaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
-10 °C

Versuchsvorschrift

Into a 250 mL round-bottomed flask was added N,N-dimethylformamide (3.5 mL) in dichloromethane (30 mL). The mixture was cooled to −10° C., and phosphoryl trichloride (4 mL) was added dropwise. The solution was warmed up to room temperature and 3,3-dimethylcyclohexanone (5.5 mL) was added slowly. The mixture was heated to reflux overnight. The reaction mixture was quenched with a 0° C. solution of sodium acetate (25 g in 50 mL water). The aqueous layer was extracted with ether (3×200 mL). The organic layers were combined, dried over Na2SO4, filtered, and dried under vacuum to give the title compound.

Aufarbeitung

  1. temperatureThe solution was warmed up to room temperature
  2. temperatureThe mixture was heated
  3. temperatureto reflux overnight
  4. customThe reaction mixture was quenched with a 0° C. solution of sodium acetate (25 g in 50 mL water)
  5. extractionThe aqueous layer was extracted with ether (3×200 mL)
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-869158c1216c45f6a24093be63d55077
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09029404B2

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