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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 223365Erstellt: 24. Oktober 2026

Propyltriphenylphosphonium bromide → 1-Carbobenzoxy-4-(1-butylidene)piperidine

https://huagongshe.com/de/reaction/223365

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropyltriphenylphosphonium bromideHCID 80374—
EduktBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Carbobenzoxy-4-(1-butylidene)piperidineHCID 20522020—

Reaktionsschritte

Butyl lithium (44 ml of 1.6 M in hexane) was added slowly to a stirred suspension of 27 g of (n-propyl)triphenylphosphonium bromide in 350 ml of tetrahydrofuran and the resulting solution was refluxed for 1 hour. The mixture was cooled in an ice bath and 18 g of N-carbobenzyloxy-4-piperidone was added. After stirring at room temperature of 0.5 hour, the solution was refluxed for 2 hours. The cooled mixture was concentrated under reduced pressure, partitioned between ether and water, and the ether layer was dried (sodium sulfate) and evaporated. The residue was filtered through silica gel with 20% ethyl acetate-hexane to give 10 g of 1-carbobenzoxy-4-(1-butylidene)piperidine as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04353900
Quelldatensatzuspto-grants-1982_10
ORD IDord-b3241550fb41428e92b1ccd841909194
Quellennotizuspto-grants-1982_10