HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564295Generated: October 30, 2026
4-Nitrophenol → 1-(1,1,2,3,3,3-Hexafluoropropoxy)-4-nitrobenzene
https://huagongshe.com/reaction/564295
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | 72414-64-3 | HCID 53471180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(1,1,2,3,3,3-Hexafluoropropoxy)-4-nitrobenzene | HCID 71365686 | 42% |
Reaction Steps
To a solution of 4.63 g of p-nitrophenol and 0.56 g of potassium hydrate added to 100 ml of N,N-dimethylformamide blowed hexafluoropropene at room temperature, and then the solution was stirred at 50° C. for 1 hour. Next, ethyl acetate and water were introduced in the reaction solution for separating the organic phase. The organic phase was dried over anhydrous sodium sulfate and the solvent was removed under a reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:EtOAc=20:1) to obtain 3.81 g of the desired product (Yield: 42%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067638B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-746c4d7cf3d848e2befd053d5d04fc02 |
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| Source note | uspto-grants-2011_11 |
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