反应详情

A solution of 7′-bromo-3′,4′-dihydrospiro[1,3-dioxolane-2,2′(1H)-naphthalene] (3.40 g, 12.6 mmol), trimethylsilylacetylene (7.0 ml, 50 mmol) (Aldrich), triphenylphosphine (0.66 g, 2.50 mmol), and palladium acetate (0.28 g, 1.25 mmol) in triethylamine (18 ml) was stirred at 70° C. for 18 hours and then concentrated in vacuo. The residue was absorbed onto silica gel from a diethyl ether solution and partially purified by elution through silica gel (15 g) with diethyl ether:hexane (1:9). Further purification by chromatography on silica gel eluting with ethyl acetate:hexane (1:19) gave 3′,4′-dihydro-7′[2-(trimethylsilyl)-ethynyl]spiro[1,3-dioxolane-2,2′(1′H)-naphthalene] (1.45 g). 1H NMR (CDCl3 200 MHz) δ: 0.23 (s, 9H, SiMe3), 1.93 (t, J=7 Hz, 2CH2), 2.95 (t, J=7 Hz, 2H, CH2), 4.02 (s, 4H, OCH2CH2O), 7.03 (d, J=8 Hz, 1H, Ar), 7.17 (s, 1H, Ar), 7.21 (d, J=8 Hz, 1H, Ar).

1. concentrationconcentrated in vacuo
2. customThe residue was absorbed onto silica gel from a diethyl ether solution
3. custompartially purified by elution through silica gel (15 g) with diethyl ether:hexane (1:9)
4. customFurther purification by chromatography on silica gel eluting with ethyl acetate:hexane (1:19)