HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259072Generated: October 30, 2026
m-Chloroperbenzoic acid → 5-Bromo-2-methylpyridin-1-ium-1-olate
https://huagongshe.com/reaction/1259072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-Bromo-2-methylpyridine | HCID 1201020 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-2-methylpyridin-1-ium-1-olate | HCID 817164 | — |
Reaction Steps
To a solution of 5-bromo-2-methylpyridine (1.0 eq.) in chloroform (0.38 M) was added 77% meta-chloroperbenzoic acid (mCPBA) (4.0 eq.) and heated at 60° C. for 20 hours. After cooling to room temperature, Ca(OH)2 (5.3 eq.) was added, and the resulting precipitate was stirred for 30 minutes. The precipitate was filtered and washed with 3:1 CHCl3/methanol. The filtrate was concentrated en vacuo to give a solid, which was stirred in 30% ethyl acetate in hexane and filtered to give the desired N-oxide. The filtrate was concentrated en vacuo, and the residue was purified by a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane to give more of the desired N-oxide. The two batches were combined and carried onto the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466167B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-af7e835f344a4a80a444f9a837f7b548 |
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| Source note | uspto-grants-2013_06 |
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