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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324971생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Phenyl-1,2,3,6-tetrahydropyridine hydrochlorideHCID 2723860—
반응물3-(Chloromethyl)-1,1'-biphenylHCID 15480892—
용매ChloroformHCID 6212—
생성물3-Phenyl[(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)methyl]benzeneHCID 15521233—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06221871B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-acaf77bd750842c2b73e4547080875d9
출처 메모uspto-grants-2001_04