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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1620924Erstellt: 26. Oktober 2026

Pyridine → (S)-Benzyl 2-(2-oxooxazolidin-4-YL)acetate

https://huagongshe.com/reaction/1620924

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktToluene-p-sulphonic anhydrideHCID 77773—
EduktPhenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoateHCID 10040985—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt(S)-Benzyl 2-(2-oxooxazolidin-4-YL)acetateHCID 11241814—

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

To a solution of the alcohol (95.7 g) from Step 1 in dichloroethane (925 mL) was added pyridine (625 mL) and the mixture was cooled to 0-5° C. Anhydrous p-toluenesulfonic anhydride (105.7 g) was added and the mixture was warmed to room temperature and stirred for 1 hour and then heated to 90° C. for 2 hours. The mixture was cooled, diluted with dichloromethane (1000 mL) and washed with 1N HCl (3×600 mL). The organic layer was washed with brine, dried with sodium sulfate and the solvents were removed in vacuo. The residue was purified by chromatography on SiO2 using ethyl acetate and hexanes in a 1:1 ratio followed by ethyl acetate to yield benzyl [(4S)-2-oxo-1,3-oxazolidin-4-yl]acetate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08772336B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-25a323c1ce15472a9ecd621f28137146
Quellennotizuspto-grants-2014_07