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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1781998Erstellt: 23. Oktober 2026

Dimethyl Sulfoxide → Benzyl 4-methylidenepiperidine-1-carboxylate

https://huagongshe.com/de/reaction/1781998

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
EduktBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
KatalysatorMethyltriphenyliphosphonium bromideHCID 74505—
ProduktBenzyl 4-methylidenepiperidine-1-carboxylateHCID 15519136—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A sodium hydride (13.2 g) was added to an anhydrous dimethylsulfoxide (176 mL) and the mixture was heated for 2 hours at 60° C. After cooling, to a suspension of methyltriphenylphosphonium bromide (110.4 g) in dimethylsulfoxide (120 mL) was added the reaction mixture, and the mixture was stirred for 30 minutes at room temperature. To the reaction mixture was added a solution of benzyl 4-oxo-1-piperidinecarboxylate (60 g) in dimethylsulfoxide (150 mL), the mixture was stirred for 1 hour at 50° C. After cooling, to the mixture was added water (2.5 L) and the mixture was extracted with ethyl acetate (1.5 L). The organic layer was washed with a saturated aqueous solution of ammonium chloride (0.5 L) and a saturated aqueous solution of sodium chloride (0.5 L), dried and then concentrated. The obtained residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate:chloroform=9:1:1) to give the title compound (51.1 g) having the following physical data.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07498323B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-976196165fb343849eb72f934f0676e2
Quellennotizuspto-grants-2009_03