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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749987Generated: October 30, 2026

Potassium Carbonate → Tert-butyl 4-(but-3-yn-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1749987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 4-(3-oxopropyl)piperidine-1-carboxylateHCID 10657745—
Reactant(1E)-1-diazo-1-dimethoxyphosphorylpropan-2-oneHCID 136023029—
SolventMethanolHCID 887—
ProductTert-butyl 4-(but-3-yn-1-yl)piperidine-1-carboxylateHCID 8668207578%

Reaction Steps

A solution of tert-butyl 4-(3-oxopropyl)piperidine-1-carboxylate (0.874 g, 3.62 mmol) in methanol (15 mL) was added with potassium carbonate (1.00 g, 7.24 mmol), and the mixture was stirred at room temperature. The reaction mixture was added with dimethyl (1-diazo-2-oxopropyl)phosphonate (0.692 g, 3.62 mmol), and the mixture was stirred at room temperature for additional 3 hours. The reaction mixture was concentrated, and then added with water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain tert-butyl 4-(but-3-ynyl)piperidine-1-carboxylate (0.670 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-fd34ec50f8a74e8f9814a279fa75cf33
Source noteuspto-grants-2015_10