反応 #1464
ord-6185c04dffd4470aa6c626e04baee724
反応方程式
反応物
反応条件
後処理
- 1workup.STIRRINGstirred for 45 min
- 2その他The resulting turbid solution was transferred, via cannula, to a flask
- 3workup.ADDITIONcontaining
- 4workup.STIRRINGThe reaction mixture was stirred for 1 h at ambient temperature and 1.5 h at 55° C
- 5抽出extracted with EtOAc (2×)
- 6洗浄The combined organic layer was washed with brine
- 7乾燥dried (MgSO4)
- 8その他The solvent was removed under reduced pressure
- 9その他the crude product was purified by flash chromatography (silica, 20% ethyl acetate in hexane)
実験手順
To a cold (-78° C.) solution of thiazole (0.38 g (0.10 mL, 1.4 mmol) in THF (2.0 mL) was added n-butyl lithium (1.6M solution in hexanes, 0.5 mL, 0.8 mmol) and stirred for 30 min. To this solution was added 0.176 g (1.3 mmol) of zinc chloride in 3.0 mL of tetrahydrofuran and stirred for 45 min. The resulting turbid solution was transferred, via cannula, to a flask containing a mixture of 0.17 g (0.35 mmol) of ethyl (E)-4-[2-(5,5-dimethyl-8-(trifluoromethylsulfonyl)oxy-5,6-dihydronaphthalen-2-yl)ethenyl]benzoate (Compound A9) and 15 mg (0.01 mmol) of tetrakis(triphenylphosphine)palladium(0) in 3.0 mL of tetrahydrofuran. The reaction mixture was stirred for 1 h at ambient temperature and 1.5 h at 55° C. The reaction mixture was treated with aqueous NH4Cl, and extracted with EtOAc (2×). The combined organic layer was washed with brine and dried (MgSO4). The solvent was removed under reduced pressure and the crude product was purified by flash chromatography (silica, 20% ethyl acetate in hexane) to afford the title compound as a white solid.