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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276480Generated: November 2, 2026

Sodium hydride → N-t-butoxycarbonyl-4-(4-fluorobenzylidene)piperidine

https://huagongshe.com/reaction/1276480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 2-oxopiperidine-1-carboxylateHCID 7577838—
ReactantDiethyl P-((4-fluorophenyl)methyl)phosphonateHCID 11064685—
Catalyst15-Crown-5HCID 36336—
SolventTetrahydrofuranHCID 8028—
ProductN-t-butoxycarbonyl-4-(4-fluorobenzylidene)piperidineHCID 2267669463.2%

Reaction Steps

A solution of 59.78 g of N-t-butoxycarbonylpiperidone and 81.25 g of diethyl 4-fluorobenzylphosphonate in 150 ml of tetrahydrofuran was added dropwise to a suspension of 13.20 g of 60% sodium hydride (in oil) containing 1.65 g of 15-crown-5 ether in 650 ml of tetrahydrofuran which was cooled in an ice bath over 20 minutes. After 1 day of stirring at room temperature, saturated aqueous sodium bicarbonate was carefully added to the reaction mixture which was subsequently extracted with ethyl acetate. The extract was washed with saturated aqueous sodium bicarbonate and saturated brine and dried over anhydrous sodium sulfate, the drying agent was removed by filtration, and then the resulting filtrate was concentrated under reduced pressure and purified by a flash column chromatography (silica gel: Wako Gel C200 (manufactured by Wako Pure Chemical Industries), eluant: hexane-ethyl acetate=20.1) to obtain 55.23 g of N-t-butoxycarbonyl-4-(4-fluorobenzylidene)piperidine. The thus obtained oily product was crystallized after its overnight standing at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166033
Source datasetuspto-grants-2000_12
ORD IDord-9edea3fbb4334906a76882d915e57f2a
Source noteuspto-grants-2000_12