HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463306Generated: October 26, 2026
Potassium Carbonate → 4-(3-Chlorophenoxy)piperidine
https://huagongshe.com/reaction/463306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[3-(Methylamino)propyl]-2-(4-fluorophenyl)-1,3-dioxolane | HCID 13335708 | — |
| Reactant | N-(2-bromoacetyl)-4-(m-chlorophenoxy)piperidine | HCID 20283061 | — |
| Reactant | 1-{N-{3-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]propyl}-N-methylaminoacetyl}-4-(3-chlorophenoxy)piperidine oxalate | HCID 20283129 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(3-Chlorophenoxy)piperidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04518713 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-36976273ec844bba84cba99274933333 |
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| Source note | uspto-grants-1985_05 |
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