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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250508Generated: October 31, 2026

Triethylamine → HCID 69971013, compound

https://huagongshe.com/reaction/1250508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,2-Dimethylhydrazine dihydrochlorideHCID 9380—
ReactantThionyl ChlorideHCID 24386—
Reactant4-Methoxy-6-[3-(trifluoromethyl)phenoxy] picolinic acidHCID 10903076—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 69971013HCID 69971013—

Reaction Steps

0.30 g (0.00096 mol) of 4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxylic acid was mixed with 0.23 g (0.00096×2.0 mol) of thionyl chloride and then with about 10 ml of benzene and a small amount of DMF, followed by treating the obtained mixture under reflux for about 30 minutes. The reaction solution was concentrated and mixed with methylene chloride. The resultant solution was dropped into a methylene chloride suspension containing 1.27 g (0.00096×10 mol) of 1,2-dimethyl hydrazine dihydrochloride and 2.03 g (0.0096×21 mol) of triethyl amine, followed by stirring the obtained solution at room temperature for about one hour. The reaction solution was distributed in ethyl acetate-saturated sodium bicarbonate water, and washed with saturated brine. The organic phase of the solution was dried with anhydrous sodium sulfate, concentrated and 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 numberUS06339045B1
Source datasetuspto-grants-2002_01
ORD IDord-76a33d86aed24b2aa802310c94f1b711
Source noteuspto-grants-2002_01