Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 15163513 | HCID 15163513 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15163460 | HCID 15163460 | 66.6% |
Reaction Steps
6.3 g of 4,5-dimethoxy-2,3-dimethylpyridine are dissolved in 120 ml of methylene chloride, 20 g of m-chloroperoxybenzoic acid are added successively and the mixture is stirred first at 20° C. for 2 hours and then at 40° C. for 4 hours. After addition of 20 ml of 5N sodium hydroxide solution, the mixture is washed three times with a mixture of 5% strength sodium thiosulphate solution and 5% strength sodium carbonate solution, the aqueous phases are back-extracted twice with methylene chloride and the combined organic phases are dried over magnesium sulphate and concentrated. 4.6 g (66% of theory) of 4,5-dimethoxy-2,3-dimethylpyridine 1-oxide are obtained. The Rf value in methylene chloride/methanol 19:1 is 0.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04686230 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-63bcfa1627524035ab17caa52c67434b |
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| Source note | uspto-grants-1987_08 |
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