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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338826Erstellt: 25. Oktober 2026

Benzyl chloroformate → (R)-benzyl 3-methyl-3-((R)-2-oxo-4-phenyloxazolidine-3-carbonyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/338826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl chloroformateHCID 10387—
EduktSodium BicarbonateHCID 516892—
Edukt(R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-oneHCID 70983198—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelHydrochloric AcidHCID 313—
Produkt(R)-benzyl 3-methyl-3-((R)-2-oxo-4-phenyloxazolidine-3-carbonyl)pyrrolidine-1-carboxylateHCID 8670739752,2%

Reaktionsschritte

To a suspension of (R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one (145.50 g, 399.25 mmol) and NaHCO3 (33.54 g, 399.25 mmol) in dry DCE (1000 mL) at ambient temperature was added dropwise a solution of benzylchloroformate (134.87 mL, 958.19 mmol) in DCE (100 mL) and the reaction was stirred at ambient temperature for 24 hours. The reaction was diluted with 1N HCl (500 mL) and the layers were separated. The organic layer was washed with 1M HCl (250 mL), dried (MgSO4), filtered and concentrated under reduced pressure to a thick yellow residue. The residue was purified by flash chromatography (5% ethyl acetate/DCM) to give (R)-benzyl 3-methyl-3-((R)-2-oxo-4-phenyloxazolidine-3-carbonyl)pyrrolidine-1-carboxylate (85.1 g, 208.35 mmol, 52.2% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889704B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-b5e7317898804ea0a861439111aac533
Quellennotizuspto-grants-2014_11