3-Furanol, tetrahydro- → 2-Methyl-4-(tetrahydro-furan-3-yloxy)-8-(2,4,6-trimethyl-phenyl)-quinoline

Beteiligte Stoffe

Reaktionsschritte

The title compound was prepared as a light yellow solid starting from 3-hydroxytetrahydrofuran and 4-chloro-2-methyl-8-(2,4,6-trimethyl-phenyl)-quinoline using procedure analogous to that described in Example 5. 1H NMR (CDCl3) δ 8.17(d,1H), 7.39-7.46(m,2H), 6.96(s,2H), 6.49(s,1H), 5.13(m,1H), 4.14(d,2H), 3.8-4.1(m,4H), 2.51(s,3H), 2.36(s,3H), 2.15-2.20(m,2H), 1.89(s,6H)ppm.

Herkunft & Nachweise