Reaktion #531841

ord-26aa30a63cd14b47a6f96d768bc7d2be

Reaktionsgleichung

C=CCc1ccc(-c2ccc(C)s2)s1
5-allyl-5′-methyl-2,2′-bithiophene
Cl[SiH](Cl)Cl
trichlorosilane
Cc1ccc(-c2ccc(CCC[Si](Cl)(Cl)Cl)s2)s1
5-(3-Trichlorosilylpropyl)-5′-methyl-2,2′-bithiophene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe hydrosilylation reaction of Example 1

Vorschrift

The hydrosilylation reaction of Example 1 was repeated using 5.0 g of 5-allyl-5′-methyl-2,2′-bithiophene in place of 2-allylthiophene, 2.5 g of anhydrous toluene, 6.0 g of trichlorosilane, and 50 mg of Platinum Catalyst. 5-(3-Trichlorosilylpropyl)-5′-methyl-2,2′-bithiophene was obtained as a colorless liquid: 1H NMR (CDCl3) δ 6.92 (d, 1H, J=3.6 Hz); 6.91 (d, 1H, J=2.7 Hz); 6.70 (d, 2H, J=3.6 Hz); 6.65 (m, 1H); 2.91 (t, 2H, J=7.2 Hz); 2.48 (d, 3H, J=1.2 Hz); 1.97 (m, 2H); 1.47 (m, 2H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08475937B2uspto-grants-2013_07