HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279189Generated: November 2, 2026
m-Chloroperbenzoic acid → HCID 18427299, compound
https://huagongshe.com/reaction/1279189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2,3-Dichloro-5-(methylthio)pyridine | HCID 15376496 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18427299 | HCID 18427299 | — |
Reaction Steps
8.9 g (0.052 mol) of m-chloroperbenzoic acid were added, a little at a time, to a suspension of 10 g (0.052 mol) of 2,3-dichloro-5-methylthiopyridine in 60 ml of methylene chloride. After the mixture had been stirred for 2 hours at approximately 20° C., a further 0.9 g (5 mmol) of m-chloroperbenzoic acid was added. The mixture was subsequently refluxed for a further 2 hours. After cooling, the solids were separated off, whereupon the organic phase was washed once with sodium hydrogen sulfite, once with sodium hydrogen carbonate and once with water. After the mixture had been dried over sodium sulfate, it was concentrated. The crude product which was obtained as a red oil was purified by means of flash chromatography over silica gel (eluent: cyclohexane/ethyl acetate=1:1). Yield: 6.3 g (58%) as a brown oil; 1H-NMR (in d6 dimethyl sulfoxide): δ [ppm]=2.9 (s, CH3); 8.4 and 8.7 (2×d, pyr H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448205B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-91d0930d33244732a9fde7ce4f754f71 |
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| Source note | uspto-grants-2002_09 |
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