Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870623Generated: October 25, 2026

Potassium Carbonate → 4-(4-Nitro-3-hydroxy-2,5,6-trifluoro-phenoxy)-4'-(4-benzyloxycarbonylphenoxy)octafluoro-biphenyl

https://huagongshe.com/reaction/1870623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium BicarbonateHCID 516893—
Reactant2,3,5,6-Tetrafluoro-4-nitrophenolHCID 611093—
Reactant4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenylHCID 10875244—
SolventDimethyl SulfoxideHCID 679—
Product4-(4-Nitro-3-hydroxy-2,5,6-trifluoro-phenoxy)-4'-(4-benzyloxycarbonylphenoxy)octafluoro-biphenylHCID 2329554892%

Reaction Steps

50 g of 4-(4-benzyloxycarbonylphenoxy)nonafluoro-biphenyl prepared as described in Example 3 (0.092 mol) and 19.4 g of 4-nitrotetrafluorophenol prepared as described in Example 4 (0.092 mol) are dissolved in 400 ml of dimethyl sulfoxide. 25 g of potassium carbonate (0.184 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 10 g of potassium hydrogencarbonate (0.1 mol) are then added. The reaction solution is ten cooled to room temperature and filtered through a fluted filter. The crude product is washed 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 numberUS06096921
Source datasetuspto-grants-2000_08
ORD IDord-ca6e8e0c5a99436caf1c2d4e076d59ec
Source noteuspto-grants-2000_08