HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425438Generated: October 30, 2026
2-Acetylpyridine → 3-(2-Bromoacetyl)pyridine hydrobromide
https://huagongshe.com/reaction/425438
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Acetylpyridine | HCID 14286 | — |
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Product | 3-(2-Bromoacetyl)pyridine hydrobromide | HCID 2776234 | — |
Reaction Steps
Acetylpyridine (120 g) is added to 33% HBr/AcOH (600 ml) with stirring (If the salt precipitates more AcOH, up to 800 ml may be added). Bromine (176 g) is added and the reaction mixture is heated to 60° C. for 2-3 h. The reaction mixture is cooled and ether (1400 ml) is added. The solid is filtered, washed with ether, and dried to give 2-bromo-1-(pyridin-3-yl)ethanone hydrobromide (Compound 13), in quantitative yield
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106209B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b411456db6ca4a1f9266ee96063740e0 |
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| Source note | uspto-grants-2012_01 |
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