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Benzyl Bromide → Dimethyl 4-benzyl-2-oxoglutarate dimethyl acetal

HRID 232220
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 232220
C([Li])CCC.C(NC(C)C)(C)C.[CH3:13][O:14][C:15]([O:26][CH3:27])([O:24][CH3:25])[C:16](=[O:23])[CH2:17][CH2:18][C:19]([O:21][CH3:22])=[O:20].[CH2:28](Br)[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.[Cl-].[NH4+]>O1CCCC1.CN(C)P(N(C)C)(N(C)C)=O>[CH3:27][O:26][C:15]([O:24][CH3:25])([O:14][CH3:13])[C:16](=[O:23])[CH2:17][CH:18]([CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:19]([O:21][CH3:22])=[O:20]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 7498Benzyl BromideHCID 7912DiisopropylamineHCID 25517Ammonium ChlorideHCID 54075676Dimethyl 2-oxoglutarate dimethyl acetalHCID 178418339Butyllithium

Produkt 1

HCID 54120089Dimethyl 4-benzyl-2-oxoglutarate dimethyl acetal

Reagenzien, Katalysatoren, Lösungsmittel

2
HCID 8028TetrahydrofuranLösungsmittel3×HCID 12679HexamethylphosphoramideLösungsmittel

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

Under nitrogen atmosphere at -78° C., 4.29 ml of 1.5 M n-butyl lithium (hexane solution) was added, while stirring, to 0.98 ml of diisopropylamine dissolved in 13 ml of anhydous tetrahydrofuran. The stirring was conducted for 15 minutes. To the resultant was added, taking 5 minutes, 1.18 g of dimethyl 2-oxoglutarate dimethyl acetal dissolved in 7 ml of anhydrous tetrahydrofuran, followed by stirring for 15 minutes. To the mixture was added, taking 5 minutes, a solution of 0.76 ml of benzyl bromide and 0.28 ml of hexamethylphosphoramide in 7 ml of anhydrous tetrahydrofuran. The mixture was stirred for 30 minutes at -78° C. The temperature of the reaction solution was raised up to -20° C. under stirring taking 2 hours, followed by addition of saturated aqueous solution of ammonium chloride, which was subjected to extraction with ethyl acetate. The extract solution was washed with water, dried (MgSO4), followed by evaporating off the solvent. The residue was subjected to a silicagel column chromalography, followed by elution with hexane-ethyl acetate (5:1→2:1) to give 1.64 g of dimethyl 4-benzyl-2-oxoglutarate dimethyl acetal as a pale yellow oily product.

Aufarbeitung

  1. additionTo the resultant was added
  2. waittaking 5 minutes
  3. additionTo the mixture was added
  4. waittaking 5 minutes
  5. stirringThe mixture was stirred for 30 minutes at -78° C
  6. stirringunder stirring
  7. waittaking 2 hours
  8. extractionwas subjected to extraction with ethyl acetate
  9. washThe extract solution was washed with water
  10. dry with materialdried (MgSO4)
  11. customby evaporating off the solvent
  12. washfollowed by elution with hexane-ethyl acetate (5:1→2:1)

Quellen und Nachweise

ORD-Eintrag
ord-5d95efa4727a4643a37a53aaf1609dd0
Quelldatensatz
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04851422

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