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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41527생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물Methyl AcrylateHCID 7294—
반응물4-Bromo-2,6-dichloroanilineHCID 69680—
반응물Sodium NitriteHCID 23668193—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylateHCID 86646793—

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530668B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-65c93b62f49045c58e2bff1318798513
출처 메모uspto-grants-2013_09