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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592130Generated: November 2, 2026

4-Fluorophenol → HCID 22599742, compound

https://huagongshe.com/reaction/1592130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
SolventDimethylformamideHCID 6228—
ProductHCID 22599742HCID 2259974267.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 2 ml of N,N-dimethylformamide were added 0.2 g of 4-chloro-6-(2-butynyloxy)pyrimidine, 0.23 g of potassium carbonate, and 0.15 g of 4-fluorophenol, followed by stirring at 60° C. for 7 hours. The reaction mixture was then left for cooling to room temperature and poured into a saturated aqueous ammonium chloride solution, which was extracted three times with chloroform. The chloroform layers were combined, washed with diluted hydrochloric acid and then with water, and dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 0.19 g of 4-(4-fluorophenoxy)-6-(2-butynyloxy)pyrimidine (the present compound (62)), m.p.: 115.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291730B2
Source datasetuspto-grants-2007_11
ORD IDord-20fdcbfa70424e399e9ed32e22660b6b
Source noteuspto-grants-2007_11