Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 6-(2,2,2-Trifluoroethoxy)-α-(trifluoromethyl)-3-pyridinemethanol | HCID 19971582 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19689334 | HCID 19689334 | — |
Reaction Steps
2.75 g (0.01 mol) of 2-(2,2,2-trifluoroethoxy)-5-(2,2,2-trifluoro-1-hydroxyethyl)-pyridine and 0.17 g (0.0005 mol) of tetrabutylammonium bromide are dissolved in 25 ml of methylene chloride at room temperature. 12.2 ml (0.012 mol) of an approximately 6% strength sodium hypochlorite solution are metered in within 10 minutes with vigorous stirring and the mixture is stirred for a further 8 hours during which the reaction temperature rises to 27° C. The reaction mixture is added to 50 ml of water, the phases are separated, the aqueous phase is extracted several times with methylene chloride and the combined organic phases are washed with saturated aqueous sodium chloride solution. After drying the organic phase with sodium sulfate, the volatiles are distilled off. Following distillation of the crude product in a kugelrohr (0.3 mbar, 100°-120° C. bath temperature), 1.31 g (48% of theory) of 2-(2,2,2-trifluoroethoxy)-5-trifluoroacetylpyridine are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05608062 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-aeb194b1d87940f8853354fcd6feec3e |
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| Source note | uspto-grants-1997_03 |
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