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HRID 2364658作成日:2026年10月26日

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

https://huagongshe.com/reaction/2364658

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 3-hydroxy-4-nitrobenzoateHCID 294866—
溶媒AcetonitrileHCID 6342—
生成物Methyl 3-allyloxy-4-nitro-benzoateHCID 5976830289%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08691822B2
出典データセットuspto-grants-2014_04
ORD IDord-363b3bd7494e49c1b823fdf9c35f537e
出典メモuspto-grants-2014_04