HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945589Generated: October 28, 2026
m-Chloroperbenzoic acid → 2-Bromo-5-methylpyridine 1-oxide
https://huagongshe.com/reaction/1945589
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Bromo-5-methylpyridine | HCID 564216 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-5-methylpyridine 1-oxide | HCID 13178737 | 91.7% |
Reaction Steps
A mixture of 2-bromo-5-methylpyridine (2.0 g, 11.6 mmol) and 3-chloroperbenzoic acid (3.0 g, 14.8 mmol) in chloroform (7 mL) was stirred at 50° C. for 3 hours, cooled down to room temperature and filtered. The filtrate was concentrated under reduced pressure to give a residue that was purified by flash chromatography (Si—PPC, MeOH:EtOAc, gradient 0:100 to 10:90) to give 2-Bromo-5-methylpyridine 1-oxide as a white solid (2.0 g, 91%). 1H NMR (400 MHz, CHCl3-d): δ 8.24 (s, 1 H); 7.52 (d, J=8.3 Hz, 1 H); 6.93 (d, J=8.33 Hz, 1 H); 2.29 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394796B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d2edd791902844359b0a36349c17f1cf |
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| Source note | uspto-grants-2013_03 |
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