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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857966Generated: November 2, 2026

Phenol → 4,5-Difluoro-6-phenoxypyrimidine

https://huagongshe.com/reaction/1857966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
Reactant4,5,6-TrifluoropyrimidineHCID 3572764—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantPotassium phenoxideHCID 23670670—
SolventTetrahydrofuranHCID 8028—
Product4,5-Difluoro-6-phenoxypyrimidineHCID 1586967468.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

With stirring, 50.4 g (0.45 mol) of potassium tert-butoxide (M=112.22) are added to a solution of 42.4 g (0.45 mol) of phenol in 400 ml of THF. The resulting potassium phenolate solution is added dropwise to a solution of 80 g (0.6 mol) of 4,5,6-trifluoropyrimidine in 1 l of THF which had been cooled to 0° C., and the mixture is stirred for 30 minutes. The solution is concentrated under reduced pressure and the residue is mixed with water and extracted with ethyl acetate. The organic phase is separated off, dried over sodium sulphate and concentrated under reduced pressure. The crude product is stirred with petroleum ether and filtered off. 63.8 g (68.1% of theory) of 5,6-difluoro-4-phenoxypyrimidine of melting point 65-66° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150374
Source datasetuspto-grants-2000_11
ORD IDord-c9ac4c0cdb5144079daf4b6d32e6173c
Source noteuspto-grants-2000_11