Tetrahydrofuran → 2-Chloro-5-(2,3-difluoro-6-methoxybenzyloxy)-4-methoxyaniline Hydrochloride

関与物質

反応手順

To a mixture of 5-chloro-2-(2,3-difluoro-6-methoxybenzyloxy)-4-nitroanisole (7.04 g), nickel(II) bromide (0.21 g), tetrahydrofuran (100 mL) and methanol (100 mL) was added sodium borohydride (2.22 g) under ice-cooling, and the mixture was stirred under ice-cooling for 30 minutes, and then stirred at room temperature for 30 minutes. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine twice, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was dissolved in ethyl acetate (20 mL). To the solution was added hydrochloric acid (4 mol/L ethyl acetate solution, 10 mL) in a dropwise manner under ice-cooling, and the mixture was stirred for 5 minutes. To the mixture was added diisopropyl ether (30 mL), and the mixture was stirred under ice-cooling for 30 minutes. The precipitated crystals were collected by filtration. The collected crystals were washed with diisopropyl ether, and dried under reduced pressure to give the title compound (6.54 g).

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