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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706476Generated: October 30, 2026

Potassium Carbonate → Tert-butyl 3-ethynyl-3-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/706476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,1-Dimethylethyl 3-formyl-3-methyl-1-piperidinecarboxylateHCID 22258917—
Reactant(1E)-1-diazo-1-dimethoxyphosphorylpropan-2-oneHCID 136023029—
SolventMethanolHCID 887—
ProductTert-butyl 3-ethynyl-3-methylpiperidine-1-carboxylateHCID 11811397573%

Reaction Steps

To a stirred solution of tert-butyl 3-formyl-3-methylpiperidine-1-carboxylate (2.10 g, 9.25 mmol) in methanol (40 mL) was added potassium carbonate (2.76 g, 20.00 mmol). The mixture was treated with dimethyl 1-diazo-2-oxopropylphosphonate (2.11 g, 11.00 mmol), and the resulting mixture was allowed to stir at room temperature. After 2 h, the mixture was concentrated, diluted with water, and extracted with ethyl acetate. The organic phase was washed with brine, dried over magnesium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (6% ethyl acetate/petroleum ether elute) to afford 1.50 g (73%) of tert-butyl 3-ethynyl-3-methylpiperidine-1-carboxylate as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174986B2
Source datasetuspto-grants-2015_11
ORD IDord-45cdf725eb83483aac013ab3b4df0d0a
Source noteuspto-grants-2015_11