HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279291Erstellt: 24. Oktober 2026
1-Chloro-4-(chloromethyl)benzene → 3-Carbamoyl-1-(4-chlorobenzyl)piperidine
https://huagongshe.com/de/reaction/279291
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
A solution of nipecotamide (6.40 g, 50 mmol) in CH3CN (150 mL) and ethanol (20 mL) was treated with Et3N (7.0 mL, 50 mmol) and 4-chlorobenzyl chloride (8.05 g, 50 mmol). The reaction mixture was stirred at 50° C. for 16 h. After cooling to room temperature, saturated aqueous NaHCO3 (50 mL) and water (150 mL) was added to the reaction mixture. The mixture was extracted with ethyl acetate (150 mL×3) and the combined organic layers were washed with brine, dried (Na2SO4) and concentrated to give a pale red solid. The crude solid was washed with ether (100 mL) to afford 3-carbamoyl-1-(4-chlorobenzyl)piperidine (6.98 g, 54%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06362177B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-6c730d6f69b54ab6a3841806aca31ca0 |
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| Quellennotiz | uspto-grants-2002_03 |
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