HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308753Generated: November 1, 2026
Potassium Carbonate → HCID 20187499, compound
https://huagongshe.com/reaction/2308753
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzylpiperidine | HCID 31738 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20187499 | HCID 20187499 | — |
Reaction Steps
A mixture of 23.35 g (0.1 mol) of 2-bromo-4'-chloroacetophenone, 17.5 g (0.1 mol) of 4-benzylpiperidine and 13.8 g (0.1 mol) of potassium carbonate in 250 ml of anhydrous ethanol is heated under reflux for 3 hours and then left to stand overnight. The inorganic materials are filtered off and washed with ethanol and the filtrate is evaporated in vacuo. A brown oily residue remains, which is triturated with diethyl ether. A solid forms and is filtered off and then washed with diethyl ether. The filtrate is collected and the solid is triturated with a mixture of dilute sodium hydroxide solution and ethyl acetate. The organic phase is separated off, washed, dried and combined with the previously obtained diethyl ether filtrate. After evaporation of the mixture in vacuo, an oil remains, which crystallises on standing and is used as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04690931 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-e7f8d96a85b948a3b811fdf41c802d1a |
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| Source note | uspto-grants-1987_09 |
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