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HRID 337192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/337192

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 nit), 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US08889722B2
出典データセットuspto-grants-2014_11
ORD IDord-461827c04cd24ae0a2de80cddea142a2
出典メモuspto-grants-2014_11