HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133583Erstellt: 24. Oktober 2026
1-Chloro-4-(chloromethyl)benzene → 3-Carbamoyl-1-(4-chlorobenzyl)piperidine
https://huagongshe.com/de/reaction/133583
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Piperidinecarboxamide | HCID 92980 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3-Carbamoyl-1-(4-chlorobenzyl)piperidine | HCID 2845797 | 55,2% |
Reaktionsschritte
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%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07390830B1 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-6f4b2841fe374baeadbc5ec0cd15c8f0 |
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| Quellennotiz | uspto-grants-2008_06 |
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