HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254063Generated: November 1, 2026
Bromine → 2-bromo-1-(6-bromopyridin-3-yl)ethanone
https://huagongshe.com/reaction/1254063
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-Acetyl-2-bromopyridine | HCID 15668195 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-bromo-1-(6-bromopyridin-3-yl)ethanone | HCID 10850267 | — |
Reaction Steps
1-(6-Bromopyridin-3-yl)ethanone was dissolved in 50 mL of chloroform and cooled to 0° C., to which was added catalytic amount of AlCl3 and 2.65 mL of bromine in 25 mL of chloroform. The addition of bromine lasted 1 h to keep the reaction solution at 0° C. After stirring at 0° C. overnight, the mixture was diluted with dichloromethane, washed with aqueous sodium bicarbonate, water, and brine. The organic layer was dried (MgSO4), filtered, and concentrated to afford 2-bromo-1-(6-bromopyridin-3-yl)ethanone which was used in the next step with out further purification. LCMS: [M+1]+=279.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455528B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-4940eecbd9234b88a4be7fbf6fac94c9 |
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| Source note | uspto-grants-2013_06 |
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