[CH:1](NC(C)C)(C)C.CN(CCN(C)C)C.[Li]CCCC.[Br:21][C:22]1[CH:23]=[CH:24][C:25]2[CH:29]=[CH:28][S:27][C:26]=2[CH:30]=1.CI>C1COCC1.C([O-])(O)=O.[Na+]>[Br:21][C:22]1[CH:23]=[CH:24][C:25]2[CH:29]=[C:28]([CH3:1])[S:27][C:26]=2[CH:30]=1Into a stirred solution of diisopropylamine (1.45 mL, 10.3 mmol) and TMEDA (3.4 mL, 22.5 mmol) in THF (30 mL, freshly distilled) at −78° C. is added 1.6 M n-BuLi (7.0 mL, 11.2 mmol) via a syringe. The solution is warmed to 0° C. for 30 min and re-cooled to −78° C. A solution of 6-bromobenzo[b]thiophene 2.0 g, 9.38 mmol) in THF (10 mL) is added via a cannula. After stirring for 30 min, a solution of CH3I (14.0 mL, 28.1 mmol, 2.0 M in tert-butyl methyl ether) is added via a cannula. The solution is stirred overnight, while allowed to warm to room temperature, and diluted with saturated aqueous NaHCO3 (50 mL). The mixture is extracted with Et2O (3×50 mL). The organic layers are combined, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a tan solid (2.0177 g, 95%).
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