Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274833Generated: October 31, 2026

Water → HCID 21249820, compound

https://huagongshe.com/reaction/1274833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 6-bromo-5-methoxypicolinateHCID 10868568—
CatalystCopper iodideHCID 83717—
SolventDimethylacetamideHCID 31374—
ProductHCID 21249820HCID 21249820—

Reaction Conditions

Temperature120 °C

Reaction Steps

3-(trifluoromethyl) phenol (1.317 g, 0.0081 mol) was dissolved in 10 ml of dried dimethyl acetamide. While cooling the obtained solution with water, sodium hydride (0.39 g (ca. 60% in mineral oil), 0.0081×1.2 mol) was added to the solution. After completion of the foaming, a solution obtained by dissolving 6-bromo-5-methoxy-2-pyridine carboxylic acid methyl ester (2.0 g, 0.0081 mol) in 10 ml of dried dimethyl acetamide, and then copper iodide (1.55 g, 0.081 mol) were successively added to the solution. The obtained mixture was heated and stirred at 120° C. for 10 hours. Thereafter, the obtained reaction solution was cooled, mixed with 50 ml of water and then with 50 ml of ethyl acetate, and filtered through a glass filter provided with Hyflo Super-Cell. The obtained filtrate was extracted with ethyl acetate to obtain an aimed product. An organic phase was separated from the product, washed with water and then dried with anhydrous sodium sulfate. The dried product was concentrated, and the obtained residues were purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159901
Source datasetuspto-grants-2000_12
ORD IDord-dad10d7ecad64392b221e69bd6dcf4dd
Source noteuspto-grants-2000_12