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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337192Generated: October 26, 2026

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

https://huagongshe.com/reaction/337192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantMethyl AcrylateHCID 7294—
Reactant4-Bromo-2,6-dichloroanilineHCID 69680—
ReactantSodium NitriteHCID 23668193—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Productmethyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylateHCID 86646793—

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889722B2
Source datasetuspto-grants-2014_11
ORD IDord-461827c04cd24ae0a2de80cddea142a2
Source noteuspto-grants-2014_11