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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72201Erstellt: 23. Oktober 2026

Pyridine → Tert-butyl (3R)-3-(methanesulfonyloxy)pyrrolidine-1-carboxylate

https://huagongshe.com/de/reaction/72201

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktEthyl AcetateHCID 8857—
EduktMethanesulfonyl chlorideHCID 31297—
Edukttert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylateHCID 854055—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl (3R)-3-(methanesulfonyloxy)pyrrolidine-1-carboxylateHCID 10934372—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

Methanesulfonyl chloride was added to a mixture of (S)-3-hydroxypyrrolidine-1-carboxylic acid tert-butyl ester (40 g) and pyridine (17.4 g) in dichloromethane (400 mL) at 0° C. The reaction mixture was stirred at this temperature for 15 min and then heated at 50° C. for 8 h. The reaction mixture was subsequently mixed with ethyl acetate and water, and the ethyl acetate phase was washed with dil. HCl solution. The ethyl acetate phase was dried over sodium sulfate and the solvent was removed in vacuo. The (R)-3-methanesulfonyloxypyrrolidine-1-carboxylic acid tert-butyl ester obtained in this way was dissolved in pyrrolidine (18.2 mL), and the reaction mixture was heated to 100° C. The reaction mixture was then mixed with ethyl acetate and water. The ethyl acetate phase was washed several times with water. The organic phase was dried over sodium sulfate and the solvent was removed in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828991B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-727bc034e03f46d881500135dc23264a
Quellennotizuspto-grants-2014_09