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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654519Erstellt: 26. Oktober 2026

Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate → Methyl 1-benzylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/654519

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
EduktBorane;tetrahydrofuranHCID 2723981—
EduktHydrochloride methanolHCID 21893726—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 1-benzylpyrrolidine-3-carboxylateHCID 461075150,2%

Reaktionsschritte

A solution of methyl 1-benzyl-2-oxo-4-pyrrolidylcarboxylate (D10, 35.4 g, 0.18 mole) in dry THF (135 ml) was added dropwise over 30 mins to 1M borane-THF solution (228 ml, 0.23 mole) at 0° C. under nitrogen, and when addition was complete the solution was heated under reflux for 1h. The solution was cooled to room temperature, then treated dropwise with 8% hydrogen chloride/methanol (114 ml, 0.25 mole HCl) and stirred for 18h, followed by 3h at reflux. The mixture was then concentrated in vacuo and the residue treated with water (40 ml), washed with ether (2×50 ml), basified with 40% sodium hydroxide solution, saturated with potassium carbonate and extracted with ether (3×70 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a yellow oil, which was purified by distillation (b.p. 146° C.0.7mm) to give the title compound (D11) as a colourless oil (19.8 g, 50%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05132316
Quelldatensatzuspto-grants-1992_07
ORD IDord-d7fce74ab2f8417f9631c77014014c0e
Quellennotizuspto-grants-1992_07