HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006058Generated: October 26, 2026
Potassium Iodide → N-phenethyl-4-(2-bromo-5-methoxy-benzyl)piperidine
https://huagongshe.com/reaction/1006058
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2-Bromo-5-methoxybenzyl)piperidine hydrochloride | HCID 22675334 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-phenethyl-4-(2-bromo-5-methoxy-benzyl)piperidine | HCID 12968865 | 58.1% |
Reaction Steps
4-(2-Bromo-5-methoxybenzyl)piperidine hydrochloride (192 mg, 0.60 mmol) was neutralized with a 1N-aqueous sodium hydroxide solution, followed by extraction with diethyl ether, whereby a corresponding free compound was obtained. A mixture of the free compound, phenethyl bromide (110 mg, 0.594 mmol), potassium carbonate (250 mg, 1.81 mmol), potassium iodide (10.3 mg, 0.062 mmol) and acetonitrile (3.6 mL) was heated under reflux under nitrogen for 8 hours. After the inorganic matters were filtered off, the filtrate was concentrated under reduced pressure and the concentration residue was purified by a flash silica gel column chromatography (hexane/ethyl acetate/triethylamine=5/15/0 to 5/15/1) to obtain N-phenethyl-4-(2-bromo-5-methoxy-benzyl)piperidine (134 mg, 58%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787560B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-eaef8a639cbc48398ec393a6080f3b49 |
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| Source note | uspto-grants-2004_09 |
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