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HRID 1531820생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1531820

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 번호US06200982B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-2de880554d7644f69b61d9ba078c0f35
출처 메모uspto-grants-2001_03