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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085916Generated: November 1, 2026

Sodium Hydroxide → 6-(2,6-Difluorophenyl)-3-(4'-trifluoromethoxybiphenyl-4-yl)-[1,2,4]triazine

https://huagongshe.com/reaction/2085916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Trifluoromethoxyphenylboric acidHCID 22727017—
Reactant3-(4-Bromophenyl)-6-(2,6-difluorophenyl)-[1,2,4]triazineHCID 22727022—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-(2,6-Difluorophenyl)-3-(4'-trifluoromethoxybiphenyl-4-yl)-[1,2,4]triazineHCID 22727026—

Reaction Conditions

Temperature70 °C

Reaction Steps

244 mg of 3-(4-bromophenyl)-6-(2,6-difluorophenyl)-[1,2,4]triazine are placed in 1.8 ml of 1,2-dimethoxyethane, and 2.5 mg of bis(triphenylphosphine)palladium(II) dichloride, 159 mg of 4-trifluoromethoxyphenylboric acid and 176 mg of sodium hydrogen carbonate in 1.8 ml of water are added in succession. The reaction mixture is then heated at 70° C. for 5 h. After cooling to room temperature, the suspension is poured into 1N sodium hydroxide solution and extracted with ethyl acetate. The organic phase is washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated. The crude product is dissolved in a minimum of hot ethyl acetate, filtered clear and crystallised at 0° C. In this way the title compound having a melting point of 199-202° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723720B2
Source datasetuspto-grants-2004_04
ORD IDord-af7f661c419e4ba2a5d2822bd3cadb51
Source noteuspto-grants-2004_04