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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382917Generated: October 31, 2026

Potassium Carbonate → 4-(4-Nitro-3-benzyloxyphenoxy)-2-(4-benzyloxycarbonylphenoxy)-3,5,6-trifluoropyridine

https://huagongshe.com/reaction/382917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium BicarbonateHCID 516893—
ReactantPotassium 4-nitro-3-benzyloxyphenoxideHCID 11781031—
Reactant2-(4-Benzyloxycarbonylphenoxy)-3,4,5,6-tetrafluoropyridineHCID 18459337—
SolventDimethyl SulfoxideHCID 679—
Product4-(4-Nitro-3-benzyloxyphenoxy)-2-(4-benzyloxycarbonylphenoxy)-3,5,6-trifluoropyridineHCID 1845933992%

Reaction Steps

40 g of the 2-(4-benzyloxycarbonylphenoxy)-3,4,5,6-tetrafluoropyridine (0.106 mol) prepared as described in Example 6 and 30 g of potassium 4-nitro-3-benzyloxyphenoxide (0.106 mol) are dissolved in 500 ml of dimethyl sulfoxide. 30 g of potassium carbonate (0.22 mol) are added in portions to the solution. The mixture is then stirred at room temperature for 24 hours, then heated at 60° C. for 24 hours, and 15 g of potassium hydrogencarbonate (0.15 mol) are then added. The reaction solution is then cooled to room temperature and filtered through a fluted filter. The crude product is extracted by shaking with 300 ml of ethyl acetate and 700 ml of water, and the organic phase is washed three times with water and evaporated in a rotary evaporator until the reaction product precipitates out. The reaction product is then recrystallized from a mixture of ethyl acetate and n-hexane (volume ratio 1:1) and then dried for 48 hours under nitrogen at 40° C./10 mbar in a vacuum drying cabinet (yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310238B1
Source datasetuspto-grants-2001_10
ORD IDord-318c779f919b4eeca960c826da2ba976
Source noteuspto-grants-2001_10