HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356745Generated: October 26, 2026
Potassium Carbonate → 2-Bromo-1-(3-pyridyl)-1-butanone
https://huagongshe.com/reaction/2356745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 1-(Pyridin-3-yl)butan-1-one | HCID 459502 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | 2-Bromo-1-(3-pyridyl)-1-butanone | HCID 86593201 | — |
Reaction Steps
To a solution of 1-(3-pyridyl)-1-butanone (20.0 g) in 47% aqueous hydrobromic acid (40 ml) and acetic acid (40 ml) was added bromine (15.2 ml), and the mixture was stirred at 60° C. for 30 minutes. The reaction mixture was poured into ice-water, and after adding a saturated aqueous sodium thiosulfate solution, potassium carbonate was added to the mixture to adjust pH to 4. The reaction mixture was extracted with ethyl acetate, washed successively with a saturated aqueous sodium hydrogen carbonate solution and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to obtain a crude product of 2-bromo-1-(3-pyridyl)-1-butanone (30.15 g) as brownish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759373B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-2ae6d71b1c624959b034eff3138e9928 |
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| Source note | uspto-grants-2010_07 |
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