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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747505Generated: November 2, 2026

Ethyl 4-piperidinecarboxylate → HCID 118020688, compound

https://huagongshe.com/reaction/1747505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant1-Bromo-4-(difluoromethoxy)benzeneHCID 2737007—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 118020688HCID 11802068856%

Reaction Conditions

Temperature80 °C

Reaction Steps

Sodium tert-butoxide (2.29 g, 23.8 mmol), palladium(II) acetate (428 mg, 1.91 mmol), and tri-tert-butylphosphine (370 μL, 1.52 mmol) were added to a solution of ethyl piperidine-4-carboxylate (3.52 mL, 22.9 mmol) and 1-bromo-4-(difluoromethoxy)benzene (4.25 g, 19.1 mmol) in toluene (122 mL), and the mixture was stirred at 80° C. for 30 minutes. Water was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with brine and then dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography [elute: hexane/ethyl acetate=100/0-90/10] to obtain the title compound (3.17 g, yield: 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150575B2
Source datasetuspto-grants-2015_10
ORD IDord-5a1039c3ce624d1d81ed159847190878
Source noteuspto-grants-2015_10