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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 2,3,5,6-Tetrafluoro-4-nitrophenol | HCID 611093 | — |
| Reactant | 4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl | HCID 10875244 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(4-Nitro-3-hydroxy-2,5,6-trifluoro-phenoxy)-4'-(4-benzyloxycarbonylphenoxy)octafluoro-biphenyl | HCID 23295548 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06096921 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-ca6e8e0c5a99436caf1c2d4e076d59ec |
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| Source note | uspto-grants-2000_08 |
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