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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylate | HCID 86646793 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-2,6-dichlorobenzaldehyde | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530668B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-bd3f4ef396a6471787c8d3eafc00f6d4 |
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| Source note | uspto-grants-2013_09 |
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