HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248773Erstellt: 25. Oktober 2026
Tetrahydrofuran → 4-Propyl-2',3'-difluoro-4'-cyanobiphenyl
https://huagongshe.com/reaction/248773
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | 1,2-Difluoro-3-trimethylsilylbenzene | HCID 10899371 | — |
| Edukt | 4-Bromo-2,3-difluorobenzonitrile | HCID 19762054 | — |
| Katalysator | HCID 178418751 | HCID 178418751 | — |
| Produkt | 4-Propyl-2',3'-difluoro-4'-cyanobiphenyl | HCID 14548490 | — |
Reaktionsschritte
0.1 mol of chlorotriisopropyl orthotitanate in 20 ml of tetrahydrofuran is added at 5° C. to a mixture of 1-bromomagnesium-4-propylbenzene (prepared from 0.1 mol of 4-propyl-bromobenzene and 0.1 mol of magnesium) and 90 ml of tetrahydrofuran and the mixture is stirred at 5° to 20° C. for 30 minutes. A mixture of 1.3 g of bis-(triphenylphosphine)-nickel(II) chloride and 0.1 mol of 4-bromo-2,3-difluorobenzonitrile (prepared from 1-trimethylsilyl-2,3-difluorobenzene by conversion into the nitrile analogously to Example 1a) 1c) and subsequent bromination with bromine with removal by distillation of the resulting trimethylsilyl bromide) is added to this mixture. Stirring for 24 hours at room temperature and customary working up gives 4-propyl-2',3'-difluoro-4'-cyanobiphenyl.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05211878 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-4679fff0ca9d4793a7eb00ae899d2e92 |
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| Quellennotiz | uspto-grants-1993_05 |
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