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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31394생성일: 2026년 10월 24일

Methanol → Methyl 3-(3-aminophenyl)isonicotinate

https://huagongshe.com/ko/reaction/31394

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Ammonium formateHCID 2723923—
반응물Methyl 3-(3-nitrophenyl)isonicotinateHCID 11276909—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-(3-aminophenyl)isonicotinateHCID 11368161—

반응 단계

Into an RBF was placed methyl 3-(3-nitrophenyl)isonicotinate (1.85 g, 7.16 mmol) and to this was added methanol (50 ml), ammonium formate (6.0 g, 35.8 mmol) and 5 wt % Pd/C (Degussa type). No initial exotherm was noticed (to the touch) and no bubbling or gas evolution was observed. After 2 h, some SM was observed to be undissolved and THF (25 ml) was added to aid in solubility. The reaction was slow at room temperature. The reaction mixture was then placed on the Buchi hydrogenator overnight. The mixture was then filtered through a pad of Celite and washed with ethyl acetate. This solution was washed with water, separated and the organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The orange oil was purified by silica gel flash chromatography using 30% ethyl acetate/Hexanes as eluent to yield 1.15 g (71% th) of an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425639B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-88a6c24cb7e3485d991292ddbe67cf3c
출처 메모uspto-grants-2008_09