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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382920Generated: October 31, 2026

Potassium Carbonate → HCID 18459338, compound

https://huagongshe.com/reaction/382920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium BicarbonateHCID 516893—
ReactantPotassium 4-nitro-3-benzyloxyphenoxideHCID 11781031—
Reactant2-(4-Benzyloxycarbonylphenoxy)-1-trifluoromethyl-3,4,5,6-tetrafluorobenzeneHCID 18459336—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 18459338HCID 1845933894%

Reaction Steps

40 g of the 2-(4-benzyloxycarbonylphenoxy)-1-trifluoromethyl-3,4,5,6-tetrafluorobenzene (0.09 mol) prepared as described in Example 9 and 25.5 g of potassium 4-nitro-3-benzyloxyphenoxide (0.09 mol) are dissolved in 400 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 and 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 allowed to cool to room temperature and is 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: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310238B1
Source datasetuspto-grants-2001_10
ORD IDord-db7e778c4dcf4d228e143bedc8a86bef
Source noteuspto-grants-2001_10