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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279351Erstellt: 25. Oktober 2026

1-Chloro-4-(chloromethyl)benzene → 3-Amino-1-(4-chlorobenzyl)homopiperidine

https://huagongshe.com/reaction/279351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-4-(chloromethyl)benzeneHCID 7723—
EduktPotassium CarbonateHCID 11430—
EduktAzepan-3-amineHCID 2756445—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-Amino-1-(4-chlorobenzyl)homopiperidineHCID 1842623993%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A solution of 3-aminohomopiperidine (1.71 g, 15 mmol) in CH3CN (45 mL) was treated with p-chlorobenzyl chloride (463 mg, 2.9 mmol) and K2CO3 (828 g, 6 mmol) and heated to 70° C. for 9 h. The reaction mixture was cooled to 25° C. and concentrated to afford a yellow solid. The residue was partitioned between H2O (5 mL) and EtOAc (50 mL), and extracted with EtOAc (2×50 mL). The combined organic extracts were washed with brine (20 mL), dried (Na2SO4) and concentrated. The resulting yellow oil was purified by chromatography (SiO2, 5-20% CH3OH—CH2Cl2 gradient elution) to afford the desired product as a yellow oil (639 mg, 93%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06362177B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-008f99bd4ef24cc2a51d056e6de3a40f
Quellennotizuspto-grants-2002_03