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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59693Erstellt: 23. Oktober 2026

Potassium bisulfate → (4S)-4-benzyl-3-(5-phenylpentanoyl)-1,3-oxazolidin-2-one

https://huagongshe.com/de/reaction/59693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium bisulfateHCID 516920—
Edukt(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
Edukt5-phenylpentanoyl ChlorideHCID 10965460—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4S)-4-benzyl-3-(5-phenylpentanoyl)-1,3-oxazolidin-2-oneHCID 1078315683%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a stirring solution consisting of (S)-4-benzyloxazolidin-2-one (0.9 g, 5.08 mmol) in THF (20 mL) at −78° C. was slowly added n-butyllithium solution (3.5 mL, 5.6 mmol, 1.6 M solution in hexane). The reaction mixture was stirred at −78° C. for two hours, after which time 5-phenylpentanoyl chloride (1 g, 5 mmol, prepared by treatment of 5-phenylpentanoic acid with oxalyl chloride and catalytic DMF) was slowly added. The reaction mixture was stirred at −78° C. for two hours and was then allowed to rise to room temperature overnight. The reaction mixture was acidified with 5% KHSO4 and extracted twice with ethyl acetate. The organic phase was washed with brine, dried over sodium sulfate, filtered, and concentrated under vacuum. The residue was purified by silica gel chromatography. Elution with ethyl acetate-heptane (25:75 v/v) afforded the title compound (1.4 g, 82%) as a clear oil; TLC Rf 0.40 (solvent system: 25:75 v/v ethyl acetate-heptane); MS (ESI+) m/z 337.4 (M+H)+, 360.2 (M+Na)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440919B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-8c0a011ccf214c169e2ed2ad5abd4a0c
Quellennotizuspto-grants-2016_09