HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133586Erstellt: 25. Oktober 2026
1-Chloro-4-(chloromethyl)benzene → {[1-(4-Chlorobenzyl)piperidin-4-yl]methyl}amine
https://huagongshe.com/reaction/133586
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-(Aminomethyl)piperidine | HCID 23527 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | {[1-(4-Chlorobenzyl)piperidin-4-yl]methyl}amine | HCID 18426145 | 69% |
Reaktionsschritte
K2CO3 (3.02 g) and 4-chlorobenzyl chloride (3.52 g, 21.8 mmol) were successively added to an acetonitrile (100 mL) solution of 4-(aminomethyl)piperidine (7.00 g, 61.3 mmol). The resulting reaction mixture was stirred at 60° C. for 16 hours, cooled to 25° C. and concentrated. The obtained residue was fractionated between dichloromethane (75 mL) and water (50 mL) and then washed with water (50 mL×2) and brine (50 mL×1). The organic layer was dried (over MgSO4), concentrated and then purified by chromatography (SiO2, 4% H2O-iPrOH) to provide 4-(aminomethyl)-1-(4-chlorobenzyl)piperidine (3.58 g, 69%).
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-f1d42b141bc340a0a10ca3237623865e |
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| Quellennotiz | uspto-grants-2008_06 |
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