Benzaldehyde → 2-Nitro-1-phenyl-1-propanol

HRID 1670861Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1670861
[CH:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N+:9]([CH2:12][CH3:13])([O-:11])=[O:10].O>O1CCCC1.C(O)(C)(C)C.CC(C)([O-])C.[K+]>[N+:9]([CH:12]([CH3:13])[CH:1]([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[OH:8])([O-:11])=[O:10]

Komponenten

7

Edukt 3

HCID 240BenzaldehydeHCID 962WaterHCID 6587Nitroethane

Produkt 1

HCID 2261182-Nitro-1-phenyl-1-propanolAusbeute 93,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23665647Potassium tert-butoxideKatalysatorHCID 6386tert-ButanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of benzaldehyde (20.0 g) and nitroethane (28.4 g) in tetrahydrofuran (50 mL) and tert-butanol (50 mL) was added potassium tert-butoxide (1.27 g) under ice-cooling, and the mixture was stirred at room temperature for 16 hr. Water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=10:1) to give the title compound as a blue oil (yield 32.0 g, 93%).

Aufarbeitung

  1. temperaturecooling
  2. extractionthe mixture was extracted with diethyl ether
  3. washThe extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=10:1)

Quellen und Nachweise

ORD-Eintrag
ord-e249ba5e12684940b9bdf0dfb32dd26c
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US07994205B2

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