反应 #9919
ord-1dcf53a9a79d4a13b5884fe5d9b1212b
溶剂
反应条件
后处理
- 1其他the reaction was quenched with methanol (1 mL)
- 2workup.ADDITIONThe solution was diluted with ether (100 mL)
- 3洗涤washed with water, saturated aqueous NaHCO3 and brine successively
- 4其他The organic layer was dried
- 5浓缩concentrated
- 6其他The residue was purified by flash chromatography on silica gel
- 7洗涤eluting with hexane
实验过程
To a solution of 7-methyl-octan-1-ol (1.20 g, 8.33 mmol) in DMF (20 mL) was added triphenylphosphine (2.43 g, 9.26 mmol). The solution was cooled to 0° C. and NBS (1.60 g, 8.99 mmol) was added in portions. After stirring for 30 min at room temperature, the reaction was quenched with methanol (1 mL). The solution was diluted with ether (100 mL), washed with water, saturated aqueous NaHCO3 and brine successively. The organic layer was dried and concentrated. The residue was purified by flash chromatography on silica gel, eluting with hexane to afford 1-bromo-7-methyl-octane (1.28 g, 74%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 3.41 (2H, t, J=6.6 Hz), 1.85 (2H, m), 1.52 (1H, m), 1.42 (2H, m), 1.28 (4H, m), 1.17 (2H, m), 0.87 (3H, s), 0.85 (3H, s); 13C NMR (75 MHz, CDCl3) δ 39.16, 34.34, 33.14, 29.34, 28.52, 28.24, 27.51, 22.94.