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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41528Generated: October 27, 2026

Dimethyl Sulfide → 4-Bromo-2,6-dichlorobenzaldehyde

https://huagongshe.com/reaction/41528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantOzoneHCID 24823—
Reactantmethyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylateHCID 86646793—
SolventDichloromethaneHCID 6344—
Product4-Bromo-2,6-dichlorobenzaldehydeHCID 56604254—

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 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530668B2
Source datasetuspto-grants-2013_09
ORD IDord-bd3f4ef396a6471787c8d3eafc00f6d4
Source noteuspto-grants-2013_09