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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275763생성일: 2026년 10월 26일

N-Methylbenzylamine → 4-(N-benzyl-N-methylaminoacetyl)pyridine

https://huagongshe.com/reaction/275763

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylbenzylamineHCID 7669—
반응물4-(Bromoacetyl)pyridine hydrobromideHCID 2776239—
용매DichloromethaneHCID 6344—
생성물4-(N-benzyl-N-methylaminoacetyl)pyridineHCID 70073631—

반응 단계

To a solution of N-benzyl-N-methylamine (3.7 cm3) in dry dichloromethane (40 cm3), cooled to 0° C. was added with stirring, 4-bromoacetylpyridine hydrobromide (4.0 g). The reaction was allowed to warm to room temperature, then stirred for a further 18 hr. The solvent was stripped at reduced pressure, and the residue partitioned between ethyl acetate and dilute aqueous Na2CO3. The organic phase was separated, dried (Na2SO4), evaporated, and the residue subjected to chromatography on silica gel, eluent 5% methanol in dichloromethane, to afford 4-(N-benzyl-N-methylaminoacetyl)pyridine, 1.49 g, 43%, as a yellow gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352994B2
출처 데이터셋uspto-grants-2002_03
ORD IDord-699ebe2269e54c3fa8fd56c24fea2b67
출처 메모uspto-grants-2002_03