Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Bromothiophene | HCID 13851 | — |
| Edukt | 5,5'-Dibromo-2,2'-bithiophene | HCID 638908 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | HCID 178418438 | HCID 178418438 | — |
| Katalysator | HCID 178418745 | HCID 178418745 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2,2':5',2'',5'',2'''-Quaterthiophene | HCID 395493 | — |
Reaktionsschritte
Thienylmagnesiumbromide, made from 13 gr (80 mmol) of T-Br and 2.43 gr (100 mmol) of magnesium in 50 ml of anhydrous ether, was added to a solution of 11.71 gr (36 mmol) of 5,5'-dibromo-2,2'-bithiophene and 100 mg (0.18 mmol) of Ni(dppp)Cl2 in 150 ml of ether. The reaction mixture was refluxed for 4 hours and subsequently poured on an ice/dilute hydrochloric acid mixture. The product was extracted with toluene and recrystallized from a mixture of toluene and ethanol. The resulting orange powder was dried in vacuo. Yield: 6,75 gr (20 mmol, 57%) of T4. M.p.: 203° C. (litt: 212). Elemental analysis: found% (theory%) C 56.49 (58.15), H 3.05 (3.05), S 37.0 (38.8). 1H-NMR (300 MHz, CDCl3): ∂=7.23 (2H, dd, J=5.0 and 1.0 Hz), ∂=7.19 (2H, dd, J=3.7 and 1.0 Hz), ∂=7.08 (4H, s), ∂=7.03 (2H, dd, J=5.0 and 3.7 Hz). M/z: 330 D (M.W.=330).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05556524 |
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| Quelldatensatz | uspto-grants-1996_09 |
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| ORD ID | ord-5c36b1f41c744aadbd163bf24bf25ecd |
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| Quellennotiz | uspto-grants-1996_09 |
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