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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561266Erstellt: 26. Oktober 2026

Methyl iodide → 1-Benzyl-3,5-dimethylpiperidin-4-one

https://huagongshe.com/reaction/561266

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt1-Benzyl-3-methyl-4-piperidoneHCID 560965—
EduktLithium HexamethyldisilazideHCID 2733832—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl-3,5-dimethylpiperidin-4-oneHCID 2227892031,5%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a −78° C. solution of 1-benzyl-3-methyl-piperidin-4-one (4.06 g, 20 mmol) in anhydrous THF (20 mL) was added lithium hexamethyldisilazide (21 mL, 21 mmol of a 1.0 M solution THF). After being stirred at −78° C. for 30 min, a solution of iodomethane (1.31 mL, 21 mmol) in THF (5 mL) was added into the reaction mixture. The resultant solution was stirred at 25° C. for 2 h and quenched with water. The aqueous layer was extracted with CH2Cl2. The organic extracts were combined, washed with brine and dried over MgSO4. The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by flash column chromatography (hexane/EtOAc) to provide 1.37 g (31.5% yield) of 1-benzyl-3,5-dimethyl-piperidin-4-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063222B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-2d3b74bdf7674fbabcccd1ce21f23f2c
Quellennotizuspto-grants-2011_11