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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324971Erstellt: 24. Oktober 2026

Triethylamine → 3-Phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzene

https://huagongshe.com/de/reaction/324971

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Phenyl-1,2,3,6-tetrahydropyridine hydrochlorideHCID 2723860—
Edukt3-(Chloromethyl)-1,1'-biphenylHCID 15480892—
LösungsmittelChloroformHCID 6212—
Produkt3-Phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzeneHCID 15521233—

Reaktionsschritte

To a solution of 45 mg of 3-chloromethylbiphenyl in 5 mL of chloroform was added 50 mg of 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride and 0.5 mL triethylamine. The reaction mixture was heated at reflux temperature overnight, cooled to room temperature, washed successively with 50 mL aliquots of dilute sodim hydroxide and brine. The chloroform was removed by evaporation under reduced pressure to yield 3-phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzene which was purified by chromatography on silica gel using 5% methanol in dichloromethane as eluent. Evaporation of the solvent yielded a solid which was treated with ethereal-HCl to give 15 mg of 3-[(4-1,2,3,6-tetrahydropyridin-1-yl)methyl]biphenyl hydrochloride (Compound 3), mp 236-238° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06221871B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-acaf77bd750842c2b73e4547080875d9
Quellennotizuspto-grants-2001_04