HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133583Generated: October 25, 2026
1-Chloro-4-(chloromethyl)benzene → 3-Carbamoyl-1-(4-chlorobenzyl)piperidine
https://huagongshe.com/reaction/133583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Piperidinecarboxamide | HCID 92980 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Carbamoyl-1-(4-chlorobenzyl)piperidine | HCID 2845797 | 55.2% |
Reaction Steps
Triethylamine (7.0 mL, 50 mmol) and 4-chlorobenzyl chloride (8.05 g, 50 mmol) were added to a solution of nipecotamide (6.40 g, 50 mmol) in acetonitrile (150 mL) and ethanol (20 mL). The resulting reaction mixture was stirred at 50° C. for 16 hours and cooled to room temperature. A saturated aqueous solution of NaHCO3 (50 mL) and water (150 mL) were then added, and the resulting mixture was extracted with ethyl acetate (150 mL×3). The extracts were washed with brine, dried over Na2SO4 and concentrated to afford a light-red solid. The obtained crude solid was washed with ether (100 mL) to provide 3-carbamoyl-1-(4-chlorobenzyl)piperidine (6.98 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07390830B1 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-6f4b2841fe374baeadbc5ec0cd15c8f0 |
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| Source note | uspto-grants-2008_06 |
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