4-fluoro-2,6-dimethylaniline

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of the compound obtained in the above step (1) (295 mg) in dichloromethane (10 mL) were added oxalyl chloride (253 μL) and a drop of N,N-dimethylformamide, and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo to give crude 2-(2-bromo-5-nitro-phenoxy)-2-methylpropionyl chloride. To a solution of 4-fluoro-2,6-dimethyl-aniline (149 mg) in tetrahydrofuran (15 mL) was added dropwise 1.6N n-butyl lithium/hexane solution (680 μL) over a period of one minute under cooling in dry ice-acetone bath under argon atmosphere. The mixture was stirred at the same temperature for 5 minutes. Thereto was added quickly a solution of 2-(2-bromo-5-nitrophenoxy)-2-methylpropionyl chloride in tetrahydrofuran (10 mL), and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture was added an aqueous citric acid solution, and the mixture was basified with an aqueous saturated sodium hydrogencarbonate solution and extracted with ethyl acetate. The organic layer was washed successively with water and brine, dried over magnesium sulfate and concentrated in vacuo. The resultant residue was purified by column chromatography on NH-silica gel (Chromatorex NH-silica gel; solvent; n-hexane/ethyl acetate=19/1→3/1) to give 2-(2-bromo-5-nitro-phenoxy)-N-(4-fluoro-2,6-dimethylphenyl)-2-methylpropionamide (262 mg) as a colorless solid. The reaction mixture was concentrated in vacuo to give crude 2-(2-bromo-5-nitro-phenoxy)-2-methylpropionyl chloride the mixture was stirred at the same temperature for 30 minutes extracted with ethyl acetate The organic layer was washed successively with water and brine dried over magnesium sulfate concentrated in vacuo The resultant residue was purified by column chromatography on NH-silica gel (Chromatorex NH-silica gel; solvent; n-hexane/ethyl acetate=19/1→3/1)

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of the compound obtained in the above step (1) (295 mg) in dichloromethane (10 mL) were added oxalyl chloride (253 μL) and a drop of N,N-dimethylformamide, and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo to give crude 2-(2-bromo-5-nitrophenoxy) -2-methylpropionyl chloride. To a solution of 4-fluoro-2,6-dimethyl-aniline (149 mg) in tetrahydrofuran (15 mL) was added dropwise 1.6N n-butyl lithium/hexane solution (680 μL) over a period of one minute under cooling in dry ice-acetone bath under argon atmosphere. The mixture was stirred at the same temperature for 5 minutes. Thereto was added quickly a solution of 2-(2-bromo-5-nitrophenoxy)-2-methylpropionyl chloride in tetrahydrofuran (10 mL), and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture was added an aqueous citric acid solution, and the mixture was basified with an aqueous saturated sodium hydrogencarbonate solution and extracted with ethyl acetate. The organic layer was washed successively with water and brine, dried over magnesium sulfate and concentrated in vacuo. The resultant residue was purified by column chromatography on NH-silica gel (Chromatorex NH-silica gel; solvent; n-hexane/ethyl acetate=19/1→3/1) to give 2-(2-bromo-5-nitro-phenoxy)-N-(4-fluoro-2,6-dimethylphenyl)-2-methylpropionamide (262 mg) as a colorless solid. The reaction mixture was concentrated in vacuo to give crude 2-(2-bromo-5-nitrophenoxy) -2-methylpropionyl chloride the mixture was stirred at the same temperature for 30 minutes extracted with ethyl acetate The organic layer was washed successively with water and brine dried over magnesium sulfate concentrated in vacuo The resultant residue was purified by column chromatography on NH-silica gel (Chromatorex NH-silica gel; solvent; n-hexane/ethyl acetate=19/1→3/1)