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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242659Erstellt: 26. Oktober 2026

Acetaldehyde → Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/242659

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetaldehydeHCID 177—
Edukt(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
ProduktTert-butyl 3-(ethylamino)pyrrolidine-1-carboxylateHCID 20800658—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of (R)-3-amino-1-N-Boc pyrrolidine (1 eq, 5.37 mmol) in methanol (20 mL) was added acetaldehyde (0.95 eq) and the resulting mixture was heated to 80° C. and stirred for 2 h., then stirred at room temperature overnight. Sodium borohydride (0.95 eq, 5.1 mmol) was added and reaction mixture was stirred for an additional 2 h. The reaction mixture was concentrated, dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate. The combined organics were washed with brine and dried over sodium sulfate. The crude product was purified on silica using hexane/ethyl acetate (10%) to hexane/ethyl acetate (50%). 1H-NMR (CDCL3) δ: 1.05 (3H, t), 1.45 (9H, s), 1.60-1.75 (1H, m), 2.00-2.10 (1H, m), 2.68 (4H, q), 2.90-3.15 (1H, m), 3.25-3.65 (4H, m). ESI-MS m/z: 215 (M+1), UV retention time: 0.75 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653096B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-6de36c0f01444b1d873210d6f2fcf513
Quellennotizuspto-grants-2014_02