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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 500053Erstellt: 24. Oktober 2026

Butanal → (R)-2-(N-Phenyl-aminooxy)-butan-1-ol

https://huagongshe.com/de/reaction/500053

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButanalHCID 261—
EduktPhosphateHCID 1061—
EduktNitrosobenzeneHCID 11473—
EduktL-ProlineHCID 145742—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(R)-2-(N-Phenyl-aminooxy)-butan-1-olHCID 1181623043%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

At about −20° C., L-proline (4 g, 34.8 mmol) was added to solution of n-butyraldehyde (25 mL, 278 mmol) and nitrosobenzene (15 g, 140 mmol) in acetonitrile (300 mL). The mixture was stirred at about −20° C. for about 48 hours, methanol (50 mL) and sodium borohydride (16 g, 432 mmol) were added, the mixture was stirred for about 10 minutes, and phosphate buffer was added. Following standard extractive workup with ethyl acetate, the crude product was purified by column chromatography with silica gel (petroleum ether-ethyl acetate =5:1, v:v, elution) to afford the title product (10.8 g, 43%). 1H NMR (300 MHz, CDCl3) δ 7.30-7.25 (m, 2H), 7.01-6.96 (m, 3H), 3.90-3.74 (m, 3H), 1.75-1.57 (m, 2H), 1.02 (t, J=7.8 Hz, 3H); LC-MS: m/z=182 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07767860B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-9c287d615b44465c8b90e329552ec1cf
Quellennotizuspto-grants-2010_08