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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822644Generated: October 26, 2026

Tetrahydrofuran → Allyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}-3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-yl)-3-hydroxyacrylate

https://huagongshe.com/reaction/1822644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant5-Chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonyl chlorideHCID 2794585—
ReactantAllyl 2-(3-(2,6-difluorophenyl)pyrazol-1-yl)acetateHCID 22169508—
ReactantPotassium butoxideHCID 23699084—
SolventWaterHCID 962—
ProductAllyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}-3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-yl)-3-hydroxyacrylateHCID 86590230—

Reaction Steps

Potassium butoxide (0.5 g) was added to a THF (10 mL) solution of allyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}acetate (0.5 g) and 5-chloro-1-methyl-3-trifluoromethylpyrazole-4-carbonyl chloride (0.44 g) at 0° C., and stirred for 5 minutes. Water (5 ml) was added thereto, and then extracted with diluted hydrochloric acid and ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, and then concentrated, and the resulting concentrate was purified through silica gel column chromatography (chloroform) to obtain the intended product, Compound No. I-133 (0.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037880B2
Source datasetuspto-grants-2006_05
ORD IDord-1b13ba0bcd2e41769c1748fcfab9e61a
Source noteuspto-grants-2006_05