反应详情

To 11.9 g (0.496 mol) of magnesium turnings in 80 mL of dry THF a solution of 50.0 g (0.239 mol) of 2-methyl-7-bromo-1H-indene and 45.0 g (0.239 mol) of 1,2-dibromoethane in 620 mL of THF was added dropwise by vigorous stirring in such rate that the mixture is refluxed. Then, this mixture was additionally refluxed for 30 minutes. Further on, to a solution of 110 g (0.853 mol) of dichlorodimethylsilane in 100 mL of THF the above-obtained solution of the Grignard reagent was added dropwise with vigorous stirring at room temperature using water bath to cool the reaction mixture. The resulting mixture was additionally stirred for 12 hours at ambient temperature, evaporated to dryness, and then 200 mL of dry ether was added. The obtained suspension was stirred for 20 minutes at room temperature and then filtered through glass frit (G3). The precipitate was additionally washed with 2×200 mL of ether. The combined filtrate was evaporated to dryness, and the residue was rectificated in vacuum, b.p. 105° C.-110° C./1 mm Hg. Yield 42.5 g (80%) of the title product. 1H NMR (CD2Cl2): δ 7.37-7.41 (m, 2H, 4,6-H), 7.30 (m, 1H, 5-H), 6.57 (m, 1H, 3-H), 3.51 (m, 2H, 1,1′-H), 2.23 (m, 3H, 2-Me), 0.81 (s, 6H, SiMe2). Anal. Calc. for C12H15ClSi: C, 64.69; H, 6.79%. Found: C, 64.56; H, 6.85%.

1. temperatureis refluxed
2. temperatureThen, this mixture was additionally refluxed for 30 minutes
3. stirringwith vigorous stirring at room temperature
4. temperatureto cool the reaction mixture
5. stirringThe resulting mixture was additionally stirred for 12 hours at ambient temperature
6. customevaporated to dryness
7. addition200 mL of dry ether was added
8. stirringThe obtained suspension was stirred for 20 minutes at room temperature
9. filtrationfiltered through glass frit (G3)
10. washThe precipitate was additionally washed with 2×200 mL of ether
11. customThe combined filtrate was evaporated to dryness