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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500053Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
ReactantPhosphateHCID 1061—
ReactantNitrosobenzeneHCID 11473—
ReactantL-ProlineHCID 145742—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(R)-2-(N-Phenyl-aminooxy)-butan-1-olHCID 1181623043%

Reaction Conditions

Temperature-20 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767860B2
Source datasetuspto-grants-2010_08
ORD IDord-9c287d615b44465c8b90e329552ec1cf
Source noteuspto-grants-2010_08