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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338827Erstellt: 25. Oktober 2026

Pyridine → (S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/338827

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDi-tert-butyl dicarbonateHCID 90495—
Edukt(S)-1-((benzyloxy)carbonyl)-3-methylpyrrolidine-3-carboxylic acidHCID 76853756—
EduktWater ammonium hydroxideHCID 86589665—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylateHCID 8670739895,6%

Reaktionsschritte

To a mixture of (S)-1-(benzyloxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid (32.87 g, 124.8 mmol), Boc2O (29.97 g, 137.3 mmol) in ethyl acetate (200 mL) was added pyridine (12.62 mL, 156.1 mmol) and the reaction mixture was stirred at ambient temperature for 3 hours. A solution of 28-30% w/w NH4OH/water (21.79 mL, 162.3 mmol) was added. The reaction was stirred at ambient temperature for 5 hours. Water (50 mL) was added. The organic layer was separated, washed with 1N HCl (50 mL) and brine, dried and concentrated under reduced pressure to give (S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylate (31.30 g, 119.3 mmol, 95.6% yield) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889704B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-a151995ce2644fc89a3d897ae133fc4c
Quellennotizuspto-grants-2014_11