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HRID 41527作成日:2026年10月23日

Hydrogen Bromide → methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylate

https://huagongshe.com/ja/reaction/41527

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物Methyl AcrylateHCID 7294—
反応物4-Bromo-2,6-dichloroanilineHCID 69680—
反応物Sodium NitriteHCID 23668193—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylateHCID 86646793—

反応条件

温度0 °C

反応手順

4-Bromo-2,6-dichloroaniline (5, 80 g) was dissolved in acetone (640 mL), and a 48% hydrogen bromide aqueous solution (120 mL) was added, followed by stirring at 0° C. A sodium nitrite (32 g) aqueous solution (160 mL) was added dropwise thereto, the mixture was stirred for 30 minutes, and methyl acrylate (200 mL), and water (200 mL) were added, followed by stirring for 1 hour. At room temperature, cuprous oxide (2 g) was added, followed by stirring for 2 hours. The reaction solution was extracted with ethyl acetate, and purified by column chromatography to obtain methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylate (48.5 g). Methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylate (48.5 g) was dissolved in dichloromethane, an ozone gas was introduced at −70° C., and ozone oxidization was performed. To the reaction solution was added dimethyl sulfide (40 mL), and this was extracted with ethyl acetate to obtain 4-bromo-2,6-dichlorobenzaldehyde (6, 37.2 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530668B2
出典データセットuspto-grants-2013_09
ORD IDord-65c93b62f49045c58e2bff1318798513
出典メモuspto-grants-2013_09