Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloro-5-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]benzaldehyde | HCID 18692932 | — |
| Reactant | Sodium;3-oxidodioxaborirane;tetrahydrate | HCID 23693097 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19068766 | HCID 19068766 | 81.5% |
Reaction Steps
38.5 g of sodium perborate tetrahydrate were added in portions over the course of 30 minutes to a solution of 16.0 g of 3-chloro-2-(4-chloro-3-formylphenyl)-5-trifluoromethylpyridine in 100 ml of glacial acetic acid at 100° C., followed by stirring at 100° C. for 1.5 hours. The mixture was cooled and then poured into 400 ml of water. The product was extracted from the aqueous phase with 3×100 ml of tert-butyl methyl ether. The combined organic phases were dried over sodium sulfate and then concentrated. The residue was triturated with n-hexane. The material insoluble in hexane was removed and extracted by boiling twice with ether, the pyridine N-oxide byproduct remaining undissolved. The combined ether phases were dried over sodium sulfate and concentrated to result in 13.7 g (81%) of colorless crystals; melting point: 149°-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05783522 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-4817f538a9ba412ca9a8994d2537bb13 |
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| Source note | uspto-grants-1998_07 |
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