HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304994Generated: October 25, 2026
Decafluorobiphenyl → 4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl
https://huagongshe.com/reaction/2304994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Decafluorobiphenyl | HCID 67949 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 23672351 | HCID 23672351 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl | HCID 10875244 | 92% |
Reaction Steps
37.4 g of decafluorobiphenyl (0.112 mol) are dissolved in 700 ml of dimethylformamide, the mixture is cooled to −10° C. using a cryostat, and a solution of 29.8 g of potassium 4-benzyloxycarbonylphenoxide (0.112mol) in 300 ml of dimethylformamide is then added dropwise over the course of 2 hours. After 48 hours at −10° C., the potassium salt has reacted. The dimethylformamide is then removed in a rotary evaporator, the residue is taken up in a little tetrahydrofuran, and the solution is filtered through a silica-gel column. The clear solution obtained is evaporated in a rotary evaporator until a white solid precipitates out. The solid is then stirred in n-hexane, filtered off using a fluted filter 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 | US06437178B2 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-4924021e330c435789a2980c8d0bf1fc |
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| Source note | uspto-grants-2002_08 |
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