HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333068Generated: October 30, 2026
m-Chloroperbenzoic acid → 2-Chloro-6-methylpyridine 1-oxide
https://huagongshe.com/reaction/333068
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 6-Chloro-2-picoline | HCID 87601 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-6-methylpyridine 1-oxide | HCID 4579772 | — |
Reaction Steps
2-Chloro-6-methylpyridine (12.76 g, 0.1 mol) was dissolved together with m-chloroperbenzoic acid (17.56 g, 0.15 mol) in DCM (100 ml) and stirred at 40° C. for 90 minutes. The heating bath was removed and stirring was continued overnight at room temperature. The reaction mixture was quenched with saturated sodium thiosulfate solution and the pH was adjusted to 8 with 1M NaOH. The phases were separated, the aqueous phase extracted with DCM and the combined organic phases were dried over magnesium sulfate. The solvent was removed under reduced pressure and unreacted 2-chloro-6-methylpyridine was removed by distillation (2 mbar, 65° C.). 2-Chloro-6-methyl-pyridine 1-oxide was obtained as residue (6.0 g of a yellow oil, 0.042 mol, 42%). MS (ESI) m/z=144.0 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877934B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-8324e3b058454acab71c208d7548a50b |
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| Source note | uspto-grants-2014_11 |
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