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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531637Generated: October 31, 2026

Water → HCID 21249825, compound

https://huagongshe.com/reaction/1531637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4,6-dichloropyridine-2-carboxylateHCID 18922464—
CatalystCopper iodideHCID 83717—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21249825HCID 21249825—

Reaction Conditions

Temperature125 °C

Reaction Steps

3-(trifluoromethyl) phenol (3.15 g, 0.0019 mol) was dissolved in 50 ml of dried dioxane. Sodium hydride (0.8 g (ca. 60% in mineral oil), 0.0019×1.05 mol) was added to the obtained solution at room temperature. After completion of the foaming, a solution obtained by dissolving 4,6-dichloro picolinic acid methyl ester (4.0 g, 0.0019 mol) in 5 ml of dried dioxane, was dropped into the above solution. Successively, copper iodide (3.7 g, 0.0019×1.0 mol) was added to the obtained solution. The resultant mixture was heated and stirred at a temperature of 120 to 130° C. for 10 hours. Thereafter, the obtained reaction solution was cooled, mixed with 10 ml of water, and then filtered through a glass filter provided with High-flow Super Cell. The obtained filtrate was extracted with 100 ml of ethyl acetate two times, thereby separating an organic phase therefrom. The obtained organic phase was dried with sodium anhydride. After the dried organic phase was subjected to distillation to remove the solvent therefrom, the obtained distillation residues were purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200933B1
Source datasetuspto-grants-2001_03
ORD IDord-446e427840214dd6ab2ef36f389d8093
Source noteuspto-grants-2001_03