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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 579528생성일: 2026년 10월 25일

Bromide ion → 1-(Pyridin-2-yl)hept-6-en-3-one

https://huagongshe.com/reaction/579528

반응식

참여 물질

역할이름HCID투입량
반응물Bromide ionHCID 259—
반응물Sodium ChlorideHCID 5234—
반응물N-methoxy-N-methyl-3-(pyridin-2-yl)propanamideHCID 78981096—
용매TetrahydrofuranHCID 8028—
생성물1-(Pyridin-2-yl)hept-6-en-3-oneHCID 66833133169.9%

반응 조건

온도0 °C

반응 단계

While under a nitrogen atmosphere, a solution of N-methoxy-N-methyl-3-(pyridin-2-yl)propanamide (1.00 g, 5.15 mmol), in tetrahydrofuran (10 mL) was cooled to 0° C. and treated with 4-butenylmagnesiun bromide (0.5 M in THF, 16 mL, 8.0 mmol) in a dropwise manner. The solution was stirred for 1 hour at 0° C. then allowed to warm to room temperature for 3 h. The resulting solution was poured into saturated aqueous sodium chloride (100 mL) and extracted with ethyl acetate (3×50 mL). The combined organic phase was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated. Purification by flash column chromatography (silica gel, 0-25% ethyl acetate in heptane) gave 1-(pyridin-2-yl)hept-6-en-3-one as a colorless oil (828 mg, 85%). ESI MS found for C12H15NO m/z [190.1 (M+1)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040703B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-8dbc8efa3b884123afc376f600b34d03
출처 메모uspto-grants-2015_05