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HRID 324971作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Phenyl-1,2,3,6-tetrahydropyridine hydrochlorideHCID 2723860—
反応物3-(Chloromethyl)-1,1'-biphenylHCID 15480892—
溶媒ChloroformHCID 6212—
生成物3-Phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzeneHCID 15521233—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06221871B1
出典データセットuspto-grants-2001_04
ORD IDord-acaf77bd750842c2b73e4547080875d9
出典メモuspto-grants-2001_04