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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252015Generated: October 25, 2026

Methanol → methyl 1-(3-chloro-2-pyridinyl)-3-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/252015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPerfluoro(methyl vinyl ether)HCID 14474—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178469376HCID 178469376—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Productmethyl 1-(3-chloro-2-pyridinyl)-3-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]-1H-pyrazole-5-carboxylateHCID 86632567—

Reaction Steps

Trifluoromethyl trifluorovinyl ether was blown into a mixture of 1.0 g of ethyl 1-(3-chloro-2-pyridinyl)-3-hydroxy-1H-pyrazole-5-carboxylate, 0.042 g of potassium hydroxide, 10 ml of methanol and 10 ml of dimethyl sulfoxide under ice-cooling. The resulting mixture was stirred at room temperature for 4 days. Water was poured into the reaction mixture, and the mixture was extracted with diethyl ether two times. The organic layers were combined, washed with water and an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel chromatography to obtain 1.32 g of methyl 1-(3-chloro-2-pyridinyl)-3-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]-1H-pyrazole-5-carboxylate of the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07867949B2
Source datasetuspto-grants-2011_01
ORD IDord-3ef1c3e3bade49ae84d7154df64a69d2
Source noteuspto-grants-2011_01