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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1674591생성일: 2026년 10월 23일

Nitric Acid → 4-(Benzyloxy)-5-methoxy-2-nitrobenzaldehyde

https://huagongshe.com/ko/reaction/1674591

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물4-(Benzyloxy)-3-methoxybenzaldehydeHCID 75506—
생성물4-(Benzyloxy)-5-methoxy-2-nitrobenzaldehydeHCID 561363—

반응 단계

4-Benzyloxy-3-methoxybenzaldehyde (4.85 g) was added to nitric acid (d=1.42, 20 mL) in a dropwise manner over 1 hour at room temperature, and this mixture was stirred for 1 hour. This reaction mixture was poured into ice water and the precipitated solid was collected by filtration. This solid was washed with water, dried under reduced pressure at 50° C. to give 4-benzyloxy-5-methoxy-2-nitrobenzaldehyde (4.99 g). To this product was added acetic acid (50 mL), followed by adding nitromethane (3.19 g) and ammonium acetate (5.36 g), and this mixture was stirred for 5 hours at 100° C. This reaction mixture was concentrated under reduced pressure. To this residue was added water and the precipitated solid was collected by filtration, and this solid was washed with methanol, dried to give 1-benzyloxy-2-methoxy-5-nitro-4-(2-nitrovinyl)benzene (4.03 g). To this compound were added benzene (96 mL), acetic acid (72 mL) and cyclohexane (24 mL), followed by adding silica gel (18 g) and iron powder (10.2 g), and this mixture was stirred at 100° C. for 1 hour. The insoluble material was removed by filtration, and this filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate/n-hexane=75/25) to give the title compound (1.06 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003647B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-6e8d8e8dac3b4e18a55057e933881a5c
출처 메모uspto-grants-2011_08