HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1870621Erstellt: 25. Oktober 2026
Decafluorobiphenyl → 4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl
https://huagongshe.com/reaction/1870621
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Decafluorobiphenyl | HCID 67949 | — |
| Edukt | Potassium | HCID 5462222 | — |
| Edukt | HCID 23672351 | HCID 23672351 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl | HCID 10875244 | — |
Reaktionsschritte
37.6 g of decafluorobiphenyl (0.112 mol) are dissolved in 700 ml of dimethylformamide, and the solution is cooled to -10° C. by means of a cryostat, and a solution of 15 g of potassium 4-benzyloxycarbonylphenoxide (0.056 mol) in 300 ml of dimethylformamide is then added drop wise 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, and the residue is taken up in a little tetrahydrofuran and filtered via a silica-gel column. The clear solution obtained is evaporated in a rotary evaporator until the reaction product precipitates out. The reaction product is then stirred in n-hexane, filtered off via a fluted filter and then dried for 48 hours under nitrogen at 40° C./10 mbar in a vacuum drying cabinet.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06096921 |
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| Quelldatensatz | uspto-grants-2000_08 |
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| ORD ID | ord-5671c9e119fa498e910f273618b32826 |
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| Quellennotiz | uspto-grants-2000_08 |
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