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Sodium hydride → HCID 57441044, Verbindung

HRID 1663663
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1663663
[C:1]([CH:3]([C:5]1[CH:6]=[C:7]([CH:12]=[CH:13][CH:14]=1)[C:8]([O:10][CH3:11])=[O:9])[CH3:4])#[N:2].C[O-].[Na+].Br[CH2:19][CH:20]1[CH2:22][CH2:21]1.[H-].[Na+]>C(#N)C.C(OCC)C>[C:1]([C:3]([C:5]1[CH:6]=[C:7]([CH:12]=[CH:13][CH:14]=1)[C:8]([O:10][CH3:11])=[O:9])([CH3:4])[CH2:19][CH:20]1[CH2:22][CH2:21]1)#[N:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 24758Sodium hydrideHCID 81503BromomethylcyclopropaneHCID 10035402Methyl 3-(1-cyanoethyl)benzoateHCID 10942334Sodium Methoxide

Produkt 1

HCID 57441044HCID 57441044, VerbindungAusbeute 6,7 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283
Diethyl Ether
Lösungsmittel
HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To a solution of methyl 3-(1-cyanoethyl)benzoate (1.5 g, 7.9=mol) in acetonitrile (20 mL) were added sodium methoxide (0.95 g, 17 mmol) and (bromomethyl)cyclopropane (1.3 g, 9.5 mmol), and the reaction mixture was stirred at room temperature for 30 min. To the reaction mixture was added sodium hydride (60% in oil, 0.7 g, 17 mmol) under ice-cooling, and the mixture was stirred at room temperature for 16 hr. The mixture was diluted with diethyl ether, and washed with 5% aqueous sodium hydrogencarbonate solution and saturated brine. The organic layer was dried over anhydrous sodium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=5/95→40/60) to give the title compound (129 mg, 6.7%) as a colorless oil.

Aufarbeitung

  1. temperaturecooling
  2. stirringthe mixture was stirred at room temperature for 16 hr
  3. washwashed with 5% aqueous sodium hydrogencarbonate solution and saturated brine
  4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  5. filtrationfiltrated
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane=5/95→40/60)

Quellen und Nachweise

ORD-Eintrag
ord-996f746b6fbc4cb39d4f3cc517c83cc6
Quelldatensatz
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08034812B2

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