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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1583653생성일: 2026년 10월 26일

Potassium hydride → N-(2-butenyl)-N-[(4-chlorophenyl)methyl]-(3-pyridyl)amine

https://huagongshe.com/reaction/1583653

반응식

참여 물질

역할이름HCID투입량
반응물Potassium hydrideHCID 82127—
반응물2-Butene, 1-bromo-HCID 122414—
반응물N-(4-Chlorobenzyl)pyridin-3-amineHCID 10036347—
용매TetrahydrofuranHCID 8028—
생성물N-(2-butenyl)-N-[(4-chlorophenyl)methyl]-(3-pyridyl)amineHCID 5451304154.7%

반응 단계

A solution of 4.4 g of N-[(4-chlorophenyl)methyl]-(3-pyridyl)amine dissolved in 50 ml of tetrahydrofuran was added to a suspension of 4 g of a 24.6% suspension of potassium hydride in oil in tetrahydrofuran. The mixture was allowed to stir at room temperature for approximately 30 minutes whereupon 4 g of 1-bromo-2-butene was added dropwise to the reaction mixture. The mixture was allowed to stir at room temperature overnight at which time the solution was evaporated to dryness. The residue was dissolved in dichloromethane and washed with water. The organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum. The oil residue was chromatographed over silica gel. Fractions containing the major component were combined and the solvent was evaporated therefrom to provide 3 g of N-(2-butenyl)-N-[(4-chlorophenyl)methyl]-(3-pyridyl)amine as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04552960
출처 데이터셋uspto-grants-1985_11
ORD IDord-c8d0fcc40cb94070ab4cc37bf1690e53
출처 메모uspto-grants-1985_11