HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006063Generated: October 31, 2026
Iodoethane → 4-(2-Bromo-5-ethoxybenzyl)-1-[(2-chlorophenyl)acetyl]piperidine
https://huagongshe.com/reaction/1006063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Bromo-5-hydroxybenzyl)-1-[(2-chlorophenyl)acetyl]piperidine | HCID 22675321 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Bromo-5-ethoxybenzyl)-1-[(2-chlorophenyl)acetyl]piperidine | HCID 22675285 | 100% |
Reaction Steps
Iodoethane (311.9 mg, 2.000 mmol) and potassium carbonate (500.0 mg, 3.619 mmol) were added to a solution (3 ml) of 4-(2-bromo-5-hydroxybenzyl)-1-[(2-chlorophenyl)-acetyl]piperidine (400.0 mg, 0.952 mmol) in N,N-dimethylformamide, and the resulting mixture was stirred at 60° C. for 3 hours. The reaction was terminated by adding water (20 ml), followed by extraction with diethyl ether. The extract layer was washed with an aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent, whereby the title compound (426.7 mg, 0.952 mmol) was quantitatively obtained.
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-ec5ac8c072cc4487a5aa1914551c65a0 |
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| Source note | uspto-grants-2004_09 |
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