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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024696Generated: October 28, 2026

Potassium Carbonate → 6-(4-Cyanophenoxy)-2-(4-trifluoromethoxyphenoxy)nicotinic acid ethyl ester

https://huagongshe.com/reaction/1024696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantp-(Trifluoromethoxy)phenolHCID 70015—
ReactantHCID 86665953HCID 86665953—
SolventDimethylformamideHCID 6228—
Product6-(4-Cyanophenoxy)-2-(4-trifluoromethoxyphenoxy)nicotinic acid ethyl esterHCID 6760576294.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Potassium carbonate (60 mg, 0.43 mmol) was added to a stirred and cooled (0° C.) solution of 2-chloro-6-(4-cyano phenoxy)nicotinic acid ethyl ester 0.13 g (0.43 mmol) in 10 ml DMF and stirred for 10 min at the same temperature. This was followed by the addition of 76.5 mg (0.43 mmol) of 4-trifluoromethoxy phenol, dissolved in 2 ml of DMF, over a period of 10 min. After the addition was completed, the contents were allowed to stir at RT. This was followed by heating for 3 h at 80° C. The reaction mixture was concentrated under reduced pressure, poured into ice-cold water and dissolved in 50 ml of ethyl acetate. Organic layer was then washed with brine solution followed by water and the crude product was purified by column chromatography using hexane:ethyl acetate (8:2) to afford 0.18 g of the required product. Percentage purity: LCMS−ve mode): 20.12%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722930B2
Source datasetuspto-grants-2014_05
ORD IDord-7a43184c2d8e43cc9265eef113be0a6c
Source noteuspto-grants-2014_05