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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349794Erstellt: 25. Oktober 2026

Ethyl trifluoromethanesulphonate → (4S,5R)-3-((S)-2-Ethyl-pentanoyl)-4-methyl-5-phenyl-oxazolidin-2-one

https://huagongshe.com/reaction/349794

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl trifluoromethanesulphonateHCID 67924—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt(4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-oneHCID 69269495—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4S,5R)-3-((S)-2-Ethyl-pentanoyl)-4-methyl-5-phenyl-oxazolidin-2-oneHCID 6926810679%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a −78° C. stirred solution of the (4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-one (9.20 g, 35.2 mmol) in dry THF (150 mL) was added NaHMDS (42.2 mL, 1.0 M in THF) dropwise. After 1 hour, ethyl trifluoromethanesulfonate (5.93 mL, 45.7 mmol) was added dropwise and the reaction was stirred at −78° C. for an additional 2 hours. The reaction was warmed to −30° C. for 30 minutes and quenched with sat. NH4Cl. The layers were separated and the aqueous layer was extracted with EtOAc (3×40 mL). The organic extracts were combined and washed with brine (2×40 mL). The organic phase was dried over MgSO4, filtered, and concentrated under reduced pressure to yield 8.05 g of crude product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179934B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-bbdfddf93c574bb091dc437a8140f82e
Quellennotizuspto-grants-2007_02