HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1395045Erstellt: 26. Oktober 2026
[4-(4-Benzoylphenyl)phenyl](phenyl)methanone → 4,4'-Bis(1-phenylethenyl)-1,1'-biphenyl
https://huagongshe.com/reaction/1395045
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | [4-(4-Benzoylphenyl)phenyl](phenyl)methanone | HCID 4671929 | — |
| Edukt | 4,4'-Bis(1-phenylethenyl)-1,1'-biphenyl | HCID 19078848 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Edukt | HCID 178444656 | HCID 178444656 | — |
| Katalysator | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4,4'-Bis(1-phenylethenyl)-1,1'-biphenyl | HCID 19078848 | — |
| Produkt | CID 53628100 | HCID 178418400 | — |
Reaktionsschritte
10.6 millimoles of n-butyllithium as a 0.53 Normal solution in benzene was admixed with 4.06 grams of methyltriphenylphosphonium bromide dissolved in 50 milliliters of tetrahydrofuran in a nitrogen-purged glass reaction vessel and the vessel maintained at ambient temperature (about 22° C.) for a period of 2 hours. A suspension of 2.05 grams of Compound VI in 30 milliliters of tetrahydrofuran was added to the reaction mixture. The reaction vessel was maintained at room temperature for a period of about 16 hours. At the end of this period, the tetrahydrofuran was evaporated and the remaining solid dissolved in a 1:1 by volume diethyl ether-water mixture. The ether and water were separated and the ether layer washed with water and subsequently the ether was evaporated. The crude product Compund VII was recrystallized twice from a 1 to 1 mixture of benzene and ethanol and the solid product obtained washed with n-hexane, the 4,4'-bis(1-phenylethenyl)1,1'-biphenyl (Compound VII) had a melting point of 193°-196° C. A benzene solution of Compound VII was prepared in a nitrogen-filled serum bottle equipped with a magnetic stirrer. The solution contained 0.5 grams (1.41 millimoles) of Compound VII and 70 milliliters of dry benzene. 7.2 milliliters of 0.482 Normal secondary butyllithium n-hexane solution was injected into the serum bottle with a hypodermic syringe to provide 3.47 milliequivalents of sec-butyllithium. The mixture was stirred at room temperature for 2 hours and 40 minutes, and resulted in a deep blue colored dispersion.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04201729 |
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| Quelldatensatz | uspto-grants-1980_05 |
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| ORD ID | ord-53f1ed5c6a6e41308db03f98a54bf335 |
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| Quellennotiz | uspto-grants-1980_05 |
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