Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759864Generated: October 26, 2026

Potassium Carbonate → 4-(2,3-Difluorobenzyloxy)-6-(2-butynyloxy)pyrimidine

https://huagongshe.com/reaction/1759864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,3-Difluorobenzyl AlcoholHCID 447153—
Reactant4-(2-Butynyloxy)-6-methanesulfonylpyrimidineHCID 22599863—
SolventDimethylformamideHCID 6228—
Product4-(2,3-Difluorobenzyloxy)-6-(2-butynyloxy)pyrimidineHCID 2259978767.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 2 ml of N,N-dimethylformamide were added 0.15 g of 4-(2-butynyloxy)-6-methanesulfonylpyrimidine, 0.14 g of potassium carbonate, and 0.16 g of 2,3-difluorobenzylalcohol, followed by stirring at 50° 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 0.13 g of 4-(2,3-difluorobenzyloxy)-6-(2-butynyloxy)pyrimidine (the present compound (76)), m.p.: 84.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838463B2
Source datasetuspto-grants-2005_01
ORD IDord-5bd59ce27ca9431f882bbd0d60dbdba6
Source noteuspto-grants-2005_01