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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53348Erstellt: 23. Oktober 2026

Ammonium Chloride → (S,E)-3-(pent-2-enoyl)-4-phenyloxazolidin-2-one

https://huagongshe.com/de/reaction/53348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2-Oxazolidinone, 4-phenyl-, (4S)-HCID 730424—
Edukt(E)-pent-2-enoyl chlorideHCID 5706546—
EduktSodium hexamethyidisilazaneHCID 45051731—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(S,E)-3-(pent-2-enoyl)-4-phenyloxazolidin-2-oneHCID 1109686328,7%

Reaktionsbedingungen

Temperatur-50 °C

Reaktionsschritte

(S)-(+)-4-Phenyl-2-oxazolidinone (4.0 g, 24 mmol, Aldrich) was dissolved in dry THF (40 mL), and the solution was cooled to -50° C. and flushed with N2. Sodium hexamethyldisilazane (1.0M in THF, 25 mL, 25 mmol) was added slowly with stirring. The compound from step 7a (2.9 g, 24 mmol) was added slowly while maintaining the temperature at -50° C., and the mixture was stirred at this temperature for 1.5 hour. The mixture was allowed to warm to 0° C. and stirred for 1 hour. Saturated aqueous NH4Cl solution was added, the mixture was stirred for 10 minutes and the mixture was extracted with methylene chloride. The extract was dried over Na2SO4, filtered and the solvent was removed. The residue was chromatographed on silica gel, eluting with 2% methanol/methylene chloride, and the product was rechromatographed with 0.5% methanol/methylene chloride to give the title compound (1.69 g). MS m/ z 246 (M+H)+, 263 (M+NH4)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05618949
Quelldatensatzuspto-grants-1997_04
ORD IDord-54fbe7df9da8436eb7d74aeb74befc5f
Quellennotizuspto-grants-1997_04