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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975204Generated: October 30, 2026

Water → HCID 19689334, compound

https://huagongshe.com/reaction/975204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-(2,2,2-Trifluoroethoxy)-α-(trifluoromethyl)-3-pyridinemethanolHCID 19971582—
ReactantSodium HypochloriteHCID 23665760—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 19689334HCID 19689334—

Reaction Steps

2.75 g (0.01 mol) of 2-(2,2,2-trifluoroethoxy)-5-(2,2,2-trifluoro-1-hydroxyethyl)pyridine and 0.18 g (0.0005 mol) of tetrabutylammonium hydrogen sulfate are dissolved in 30 ml of methylene chloride at room temperature. 22 ml (0.036 mol) of an approximately 12% strength sodium hypochlorite solution are metered in within 10 minutes with vigorous stirring and the mixture is stirred for a further 4.5 hours during which the reaction temperature rises to 25° 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), 2.48 g (90% of theory) of 2-(2,2,2-trifluoroethoxy)-5-trifluoroacetylpyridine are obtained, which, according to GC, is 96% pure. nD20 : 1.4312.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608062
Source datasetuspto-grants-1997_03
ORD IDord-f8126f82640f450092fdcdee3ec00db8
Source noteuspto-grants-1997_03