Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1694407Erstellt: 26. Oktober 2026

Pyrrolidine → 1-(3,5-Difluorobenzyl)pyrrolidine

https://huagongshe.com/reaction/1694407

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyrrolidineHCID 31268—
EduktSodium BicarbonateHCID 516892—
Edukt3,5-DifluorobenzaldehydeHCID 588160—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(3,5-Difluorobenzyl)pyrrolidineHCID 6727925274%

Reaktionsschritte

3,5-Difluorobenzaldehyde (2.0 mL, 18.24 mmol), pyrrolidine (1.8 mL, 21.56 mmol), and sodium triacetoxyborohydride (5.8 g, 27.4 mmol) were stirred in THF (50 mL) for 16 h at room temperature. Saturated aqueous NaHCO3 (30 mL) was added and after stirring for 30 min, EtOAc (50 mL) was added. The organic phase was separated and washed with brine, dried over MgSO4 and concentrated to afford 2.65 g (74%) of 1-(3,5-difluorobenzyl)pyrrolidine as a slightly cloudy oil: 1H NMR (CDCl3) δ 6.88-6.83 (m, 1H), 6.68-6.63 (m, 2H), 3.59 (s, 2H), 2.53-2.48 (m, 4H), 1.80-1.77 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08158673B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-2090fbbe074e4ccebf96bc4aa6be1629
Quellennotizuspto-grants-2012_04