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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592230Generated: October 30, 2026

2-Chlorophenol → HCID 22599858, compound

https://huagongshe.com/reaction/1592230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorophenolHCID 7245—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(2-Butynyloxy)-5-fluoro-6-chloropyrimidineHCID 22599717—
SolventDimethylformamideHCID 6228—
ProductHCID 22599858HCID 2259985882.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 2 ml of N,N-dimethylformamide were added 0.1 g of 4-chloro-6-(2-butynyloxy)-5-fluoropyrimidine, 0.1 g of potassium carbonate, and 0.08 g of 2-chlorophenol, followed by stirring at 60° C. for 1 hour. The reaction mixture was left for cooling to room temperature and poured into a saturated aqueous ammonium chloride solution, which was extracted three times with t-butyl methyl ether. The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.12 g of 4-(2-butynyloxy)-6-(2-chlorophenoxy)-5-fluoropyrimidine (the present compound (184)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291730B2
Source datasetuspto-grants-2007_11
ORD IDord-278b8254e2ba43bc942e8cda2fc58f99
Source noteuspto-grants-2007_11