Dimethylformamide → HCID 178439837, compound

Participants

Reaction Conditions

Reaction Steps

To a solution 1-allyldimethylsilyl-4-bromo-naphthalene (1 Scheme 26, 3.0 g, 10 mmol) in dry THF (150 mL) at −78° C. was added t-butyllithium (6.0 mL, 1.7 M solution in pentane, 10.2 mmol) over a period of 10 min. After 30 min stirring at −78° C., anhydrous DMF (1.5 mL, 20 mmol) was added dropwise. The reaction mixture was stirred further for 1 h and warmed to room temperature. Concentrated NH4Cl (5 mL) was added to the solution, and the reaction mixture was concentrated. The residue was extracted with ethyl acetate (50 mL) and brine (10 mL), and the organic layer was dried (Na2SO4), concentrated. The crude product was purified by column chromatography (1:20 ethyl acetate/hexanes) to afford a colorless oil (2.1 g, 88%); 1H NMR (300 MHz, CDCl3) δ 0.53 (s, 6 H), 2.03 (d, J=7.80 Hz, 2 H), 4.88-4.97 (2 H), 5.79 (m, 1 H), 7.60-7.70 (2 H), 7.84 (d, J=7.50 Hz, 1 H), 7.89 (d, J=6.90 Hz, 1 H), 8.20 (d, J=8.10 Hz, 1 H), 9.35 (d, J=8.10 Hz, 1 H), 10.39 (s, 1 H); 13C NMR (75 MHz, CDCl3) −1.7 (2C), 24.2, 114.5, 126.1, 126.9, 128.6, 128.7, 132.9, 134.3, 135.4, 137.6, 146.8, 194.1.

Provenance & Evidence