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3-bromo-N-methoxy-N,2-dimethylbenzamide → 1-(3-Bromo-2-methylphenyl)-1-pentanone

HRID 1391793
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1391793
[Br:1][C:2]1[C:3]([CH3:14])=[C:4]([CH:11]=[CH:12][CH:13]=1)[C:5](N(C)OC)=[O:6].[CH2:15]([Mg]Cl)[CH2:16][CH2:17][CH3:18]>C1COCC1>[Br:1][C:2]1[C:3]([CH3:14])=[C:4]([C:5](=[O:6])[CH2:15][CH2:16][CH2:17][CH3:18])[CH:11]=[CH:12][CH:13]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 218861973-bromo-N-methoxy-N,2-dimethylbenzamideHCID 178418265HCID 178418265, Verbindung

Produkt 1

HCID 586298971-(3-Bromo-2-methylphenyl)-1-pentanoneAusbeute 28 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of 3-bromo-N,2-dimethyl-N-(methyloxy)benzamide (2.55 g, 9.88 mmol) in anhydrous THF (28 mL) under nitrogen at −78° C. was added a butylmagnesium chloride (20% wt in THF/toluene, 6.94 mL, 11.90 mmol) drop-wise over 15 min. The resulting solution was stirred at −78° C. for 1 h, was allowed to warm to 0° C. and then stirred with slow warming to ambient temperature over 20 h. The reaction was then quenched with water (50 mL) and extracted with EtOAc (2×60 mL). Some saturated aqueous NH4Cl was added to disperse the emulsion formed. The resulting organic layer was then washed with brine (100 mL), dried (Na2SO4), filtered and reduced under vacuum. Purification by SPE (silica, 50 g cartridge), eluting with cyclohexane:EtOAc (gradient 49:1 to 9:1) afforded the title compound as a colourless oil (706 mg).

Aufarbeitung

  1. temperatureto warm to 0° C.
  2. stirringstirred
  3. temperaturewith slow warming to ambient temperature over 20 h
  4. customThe reaction was then quenched with water (50 mL)
  5. extractionextracted with EtOAc (2×60 mL)
  6. additionSome saturated aqueous NH4Cl was added
  7. additionto disperse the emulsion
  8. customformed
  9. washThe resulting organic layer was then washed with brine (100 mL)
  10. dry with materialdried (Na2SO4)
  11. filtrationfiltered
  12. customPurification by SPE (silica, 50 g cartridge)
  13. washeluting with cyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-e4860e1aa2e9417da1cf71ecb4a48891
Quelldatensatz
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07338960B2

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