HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133628Erstellt: 25. Oktober 2026
1-Chloro-4-(chloromethyl)benzene → 3-Amino-1-(4-chlorobenzyl)homopiperidine
https://huagongshe.com/reaction/133628
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Azepan-3-amine | HCID 2756445 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3-Amino-1-(4-chlorobenzyl)homopiperidine | HCID 18426239 | 93% |
Reaktionsschritte
p-Chlorobenzyl chloride (463 mg, 2.9 mmol) and K2CO3 (828 g, 6 mmol) were added to an acetonitrile (45 mL) solution of 3-aminohomopiperidine (1.71 g, 15 mmol), and the resulting mixture was stirred at 70° C. with heating for 9 hours, cooled to 25° C. and concentrated to afford a yellow solid. The resulting residue was partitioned between H2O (5 mL) and ethyl acetate (50 mL) and the aqueous layer was extracted with ethyl acetate (50 mL×2). The organic layers were combined, washed with brine (20 mL), dried (over MgSO4) and concentrated. The obtained yellow oil was purified by column chromatography (SiO2, 5-20% methanol/dichloromethane gradient elution) to afford the objective compounds as yellow oil (639 mg, 93%).
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-604b89e912b449709603e513eb5f83ed |
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| Quellennotiz | uspto-grants-2008_06 |
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