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HRID 41527Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktMethyl AcrylateHCID 7294—
Edukt4-Bromo-2,6-dichloroanilineHCID 69680—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produktmethyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylateHCID 86646793—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530668B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-65c93b62f49045c58e2bff1318798513
Quellennotizuspto-grants-2013_09