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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32837Erstellt: 23. Oktober 2026

Acetic Acid → HCID 86603396, Verbindung

https://huagongshe.com/de/reaction/32837

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2,4,6-Triisopropylbenzenesulfonyl azideHCID 371707—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
Edukt4-Phenyl-3-(3-phenyl-butyryl)-oxazolidin-2-oneHCID 10357976—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 86603396HCID 8660339641%

Reaktionsschritte

Potassium bis(trimethylsilyl)amide (2.0 mL, 1.8 mmol, 0.91 M in tetrahydrofuran) was added to (S)-4-phenyl-3-((S)-3-phenyl-butyryl)-oxazolidin-2-one (500 mg, 1.6 mmol) in anhydrous tetrahydrofuran (8 mL) at −78° C. and stirred for 1 hour. In a separate flask, a solution of 2,4,6-triisopropylbenzenesulphonyl azide (625 mg, 2.0 mmol) in anhydrous tetrahydrofuran (10 mL) at −78° C. was added via cannula to the anion at −78° C. and stirring continued for 2 hours. Acetic acid (0.45 mL, 7.8 mmol) was added to the reaction at −78° C., the mixture warmed to room temperature and stirred overnight. The mixture was poured into water (30 mL) and extracted with ethyl acetate. The combined extracts were washed with brine and dried over sodium sulfate. The crude product was purified on silica gel with 2:1 dichloromethane/hexane to give (S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-one (230 mg, 41%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07427635B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-63ca72f3d4f24e16ba1c51f65551f18a
Quellennotizuspto-grants-2008_09