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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234120Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/234120

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
PatentnummerUS05594141
Quelldatensatzuspto-grants-1997_01
ORD IDord-3006b2ef9eb540e48e8c70bd67547adc
Quellennotizuspto-grants-1997_01