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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275763Erstellt: 26. Oktober 2026

N-Methylbenzylamine → 4-(N-benzyl-N-methylaminoacetyl)pyridine

https://huagongshe.com/reaction/275763

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-MethylbenzylamineHCID 7669—
Edukt4-(Bromoacetyl)pyridine hydrobromideHCID 2776239—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(N-benzyl-N-methylaminoacetyl)pyridineHCID 70073631—

Reaktionsschritte

To a solution of N-benzyl-N-methylamine (3.7 cm3) in dry dichloromethane (40 cm3), cooled to 0° C. was added with stirring, 4-bromoacetylpyridine hydrobromide (4.0 g). The reaction was allowed to warm to room temperature, then stirred for a further 18 hr. The solvent was stripped at reduced pressure, and the residue partitioned between ethyl acetate and dilute aqueous Na2CO3. The organic phase was separated, dried (Na2SO4), evaporated, and the residue subjected to chromatography on silica gel, eluent 5% methanol in dichloromethane, to afford 4-(N-benzyl-N-methylaminoacetyl)pyridine, 1.49 g, 43%, as a yellow gum.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352994B2
Quelldatensatzuspto-grants-2002_03
ORD IDord-699ebe2269e54c3fa8fd56c24fea2b67
Quellennotizuspto-grants-2002_03