HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308767Generated: October 31, 2026
Potassium Carbonate → HCID 20187482, compound
https://huagongshe.com/reaction/2308767
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-[(4-Fluorophenyl)methyl]piperidine hydrochloride | HCID 17039492 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20187482 | HCID 20187482 | — |
Reaction Steps
78 ml of ethanol are placed in a 250 ml conical flask and 2 ml of a 5.3N methanolic solution of sodium methoxide are added. 2.29 g (0.01 mol) of 4-(4-fluorobenzyl)-piperidine hydrochloride are added and the mixture is stirred for 15 minutes. 1.38 g of potassium carbonate are then added, followed by 2.33 g (0.01 mol) of 2-bromo-4'-chloroacetophenone, and the mixture is heated under reflux for 2 hours. It is left to cool, the inorganic precipitate is filtered off, the filtrate is evaporated to dryness and the residual oil is taken up in 1N hydrochloric acid. Extraction is carried out with chloroform and the organic phase is washed with water, dried over sodium sulphate and evaporated to dryness. 3.22 g of the crude hydrochloride remain in the form of an oil, which is used as such but which can be recrystallized from a mixture of acetone/diethyl ether (melting point=168° C.).
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-ae1151cc01d34c8aba06d7e73314473c |
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| Source note | uspto-grants-1987_09 |
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