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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458757Generated: October 29, 2026

Tetrahydrofuran → 1-Boc-4-Methylenepiperidine

https://huagongshe.com/reaction/458757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventEthyl AcetateHCID 8857—
SolventHCID 178418244HCID 178418244—
Product1-Boc-4-MethylenepiperidineHCID 2756808—

Reaction Steps

To a solution of 986 mg of methyltriphenylphosphonium bromide in 20 ml of tetrahydrofuran, 1.87 ml of 1.63 M n-butyl lithium/hexane solution was added dropwise at 0° C., under cooling with ice. The temperature then was immediately raised to room temperature, and the system was stirred for 50 minutes. The reaction liquid was again cooled to 0° C., to which a solution of 500 mg of t-butyl 4-oxotetrahydropyridine-1(2H)-carboxylate in 5 ml of tetrahydrofuran was added dropwise, followed by an hour's stirring at the same temperature. The reaction liquid was diluted with ethyl acetate, washed successively with saturated aqueous ammonium chloride solution and saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the resulting residue was purified on silica gel column chromatography (eluent: hexane/ethyl acetate=5/1) to provide 192 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192969B2
Source datasetuspto-grants-2007_03
ORD IDord-a70eb147709e4184a9e681b26e15ce89
Source noteuspto-grants-2007_03