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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2406603생성일: 2026년 10월 25일

1-Phenyl-2-(4-pyridinyl)ethanone → 1-Phenyl-2-(pyridin-4-yl)ethanamine

https://huagongshe.com/reaction/2406603

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenyl-2-(4-pyridinyl)ethanoneHCID 287104—
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
용매DichloromethaneHCID 6344—
생성물1-Phenyl-2-(pyridin-4-yl)ethanamineHCID 1046534278.8%
생성물Ammonia methanolHCID 2170589710%

반응 조건

온도80 °C

반응 단계

A mixture of (2) (1.98 g, 10.0 mmol), ammonium acetate (23.2 g, 300 mmol), and sodium cyanoborohydride (4.63 g, 69.9 mmol) in EPA (100 mL) was heated at 80° C. overnight. The mixture was evaporated under reduced pressure to remove IPA. The residue was diluted with water, and basified with NaOH (2M) to pH>7. The aqueous layer was extracted with dichloromethane (3×). The pooled organic layer was removed under vacuum. The residue was purified by chromatography on silica gel (100% ethyl acetate, then 10% saturated ammonia methanol in dichloromethane) to give 1-phenyl-2-(pyridin-4-yl)ethanamine (3) as a clear oil (0.780 g, 3.94 mmol, 39% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08809379B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-ab67822c53f44edd963ba7fa5ec2c3db
출처 메모uspto-grants-2014_08