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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78732Erstellt: 24. Oktober 2026

(S)-2-(Boc-Amino)-N-methoxy-n-methylbutyramide → tert-butyl N-((2S)-1-oxobutan-2-yl)carbamate

https://huagongshe.com/de/reaction/78732

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(S)-2-(Boc-Amino)-N-methoxy-n-methylbutyramideHCID 10422029—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelDiethyl EtherHCID 3283—
Produkttert-butyl N-((2S)-1-oxobutan-2-yl)carbamateHCID 10241556—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of LiAlH4 (0.453 g, 11.9 mmol) in Et2O (20 mL) at 0° C. was added dropwise a solution of 1,1-dimethylethyl ((1S)-1-{[methyl(methyloxy)amino]carbonyl}-propyl)carbamate (2.67 g, 10.8 mmol) in Et2O (15 mL). The reaction mixture was stirred for 30 min at 0° C. and quenched with EtOAc (6.5 mL) followed by 5% aq. potassium bisulfate (6.5 mL). The reaction mixture was washed with 1 M aq. HCl (3×10 mL), saturated aq. NaHCO3 (3×10 mL), and brine (10 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to afford the title compound as a clear, colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841463B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-5760667bccfa440ab1833c283b8e4596
Quellennotizuspto-grants-2014_09