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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223365Generated: October 27, 2026

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

https://huagongshe.com/reaction/223365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyltriphenylphosphonium bromideHCID 80374—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Carbobenzoxy-4-(1-butylidene)piperidineHCID 20522020—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04353900
Source datasetuspto-grants-1982_10
ORD IDord-b3241550fb41428e92b1ccd841909194
Source noteuspto-grants-1982_10