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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463306Generated: October 26, 2026

Potassium Carbonate → 4-(3-Chlorophenoxy)piperidine

https://huagongshe.com/reaction/463306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[3-(Methylamino)propyl]-2-(4-fluorophenyl)-1,3-dioxolaneHCID 13335708—
ReactantN-(2-bromoacetyl)-4-(m-chlorophenoxy)piperidineHCID 20283061—
Reactant1-{N-{3-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]propyl}-N-methylaminoacetyl}-4-(3-chlorophenoxy)piperidine oxalateHCID 20283129—
SolventEthanolHCID 702—
Product4-(3-Chlorophenoxy)piperidineHCID 2735317—

Reaction Steps

To a suspension of 2-[3-(methylamino)propyl]-2-(4-fluorophenyl)-1,3-dioxolane (7.2 g, 30.0 mmol), potassium carbonate (10.6 g, 76.8 mmol) and 120 ml of ethanol at 0° was added dropwise a solution of N-(2-bromoacetyl)-4-(3-chlorophenoxy)piperidine (11.3 g, 34.0 mmol) in 120 ml of ethanol. The solution was stirred 1 hour at room temperature and at reflux for 1 hour. The mixture was poured into saturated sodium bicarbonate, extracted with methylene chloride, washed with water and dried over magnesium sulfate. Filtration followed by evaporation of the solvent provided an oil. Yield: 11.0 g of 1-{N-{3-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]propyl}-N-methylaminoacetyl}-4-(3-chlorophenoxy)piperidine oxalate. Yield from 4-(3-chlorophenoxy)piperidine: 43%; from N-(2-bromoacetyl)-4-(3-chlorophenoxy)piperidine: 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518713
Source datasetuspto-grants-1985_05
ORD IDord-36976273ec844bba84cba99274933333
Source noteuspto-grants-1985_05