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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 215947Erstellt: 25. Oktober 2026

Allyl iodide → 1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/215947

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl iodideHCID 11166—
Edukt1-Benzyl 4-methyl piperidine-1,4-dicarboxylateHCID 1512544—
EduktLithium HexamethyldisilazideHCID 2733832—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylateHCID 5889318691%

Reaktionsbedingungen

Temperatur-50 °C

Reaktionsschritte

Lithium bis(trimethylsilyl)amide (LiHMDS) in THF (1.0 M, 45 mL) was added to a solution of 1-benzyl 4-methyl piperidine-1,4-dicarboxylate (10.0 g, 0.0360 mol) at −78° C. The reaction mixture was slowly warmed to −50° C. and kept at this temperature for 10 min, and then re-cooled to −78° C. 3-Iodo-1-propene (4.95 mL, 0.0541 mol) was added slowly. After the addition, the mixture was allowed to warm slowly to room temperature and kept at room temperature for 3 hours. The mixture was carefully quenched (the pH was adjusted to 4) with 1N HCl solution, and ethyl acetate (200 mL) was added. The organic layer was separated and washed with water, NaHCO3 (7.5%), brine, dried over MgSO4, and filtered. The filtrate was concentrated. The residue was purified by flash chromatography with 20% ethyl acetate in hexane to give 1-benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate (10.4 g, 90.9%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193207B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-98fd19bc7d554feaaaa0296872952538
Quellennotizuspto-grants-2012_06