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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2364658생성일: 2026년 10월 25일

Allyl bromide → Methyl 3-allyloxy-4-nitro-benzoate

https://huagongshe.com/reaction/2364658

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 3-hydroxy-4-nitrobenzoateHCID 294866—
용매AcetonitrileHCID 6342—
생성물Methyl 3-allyloxy-4-nitro-benzoateHCID 5976830289%

반응 단계

Methyl 3-hydroxy-4-nitro-benzoate 1b (7 g, 35.50 mmol) was dissolved in 100 mL of anhydrous acetonitrile followed by the addition of potassium carbonate (14.70 g, 106.50 mmol) and 3-bromopropene (6.2 mL, 71 mmol) successively, the reaction mixture was heated to reflux for 3 hours with stirring. The resulting mixture was filtered and the filtrate was concentrated under reduced pressure. The crude residue was added with 150 mL of ethyl acetate, washed with water (100 mL×3) and saturated sodium chloride solution (100 mL×3) successively, then dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound methyl 3-allyloxy-4-nitro-benzoate 1c (7.45 g, yield: 89.0%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691822B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-363b3bd7494e49c1b823fdf9c35f537e
출처 메모uspto-grants-2014_04