Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354113Generated: November 2, 2026

Sodium hydride → HCID 17979083, compound

https://huagongshe.com/reaction/1354113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactant3,3,3-Trifluoro-2-methyl-2-(trifluoromethyl)propan-1-olHCID 2736185—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17979083HCID 17979083—

Reaction Steps

In 4 ml of tetrahydrofuran was suspended 0.11 g of sodium hydride (60% in oil), to which 0.5 ml of a solution containing 0.44 g of 2,2-bis(trifluoromethyl)propanol in tetrahydrofuran was added dropwise at room temperature, followed by stirring for 10 minutes. To this was added dropwise 0.5 ml of a solution containing 0.3 g of 4,6-dichloropyrimidine in tetrahydrofuran at 0° C., followed by stirring at the same temperature for 1.5 hours. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution, which was extracted three times with t-butyl methyl ether. The combined organic layers were washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate to give a crude product of 4-chloro-6-[2,2-bis(trifluoromethyl)propoxy]pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223769B2
Source datasetuspto-grants-2007_05
ORD IDord-aaa4e59837a94842b44ac3776c5ca36f
Source noteuspto-grants-2007_05