2-(4-甲基磺酰基苯基)乙酰基 氯化物

反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: Thereafter 102 g (0.765 mole) of anhydrous aluminum chloride was suspended in 200 ml of fluorobenzene. To the suspension was added dropwise a suspension of 120 g of the 4-methylsulfonylphenylacetyl chloride obtained above in 200 ml of fluorobenzene at a temperature of 0° to 3° C. The reaction vessel used was rinsed with 30 ml of fluorobenzene and the mixture was stirred at 20° C. for 4 hours. The reaction mixture was gradually poured into a mixture of ice water and hydrochloric acid and left to stand overnight, giving gummy solids. The solids were collected by filtration. The organic layer was separated from the filtrate and subjected to distillation under reduced pressure to recover 200 ml (52%) of fluorobenzene. The gummy solids were dissolved in dichloromethane, washed sequentially with water, a 5% aqueous solution of sodium bicarbonate and a saturated saline solution and dried over magnesium sulfate. The dichloromethane was distilled off and the resulting crystals were washed with diethyl ether, giving 77 g (51%) of 1-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)ethanone as pale yellow solids. To the suspension was added dropwise The reaction vessel used was rinsed with 30 ml of fluorobenzene The reaction mixture was gradually poured into a mixture of ice water and hydrochloric acid left to stand overnight giving gummy solids The solids were collected by filtration The organic layer was separated from the filtrate subjected to distillation under reduced pressure to recover 200 ml (52%) of fluorobenzene The gummy solids were dissolved in dichloromethane washed sequentially with water a 5% aqueous solution of sodium bicarbonate and a saturated saline solution and dried over magnesium sulfate The dichloromethane was distilled off the resulting crystals were washed with diethyl ether

反应条件: temp:90.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: First, a mixture of 110 g (0.51 mole) of 4-methylsulfonylphenylacetic acid and 110 ml (1.51 moles) of thionyl chloride was heated at 90° C. for 2 hours. After completion of the reaction, an excess of thionyl chloride was distilled off under reduced pressure, giving about 120 g of 4-methylsulfonylphenylacetyl chloride as a light brown solid. The solid thus obtained was subjected to the subsequent reaction without isolation and purification. After completion of the reaction an excess of thionyl chloride was distilled off under reduced pressure

反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: Thereafter 102 g (0.765 mole) of anhydrous aluminum chloride was suspended in 200 ml of fluorobenzene. To the suspension was added dropwise a suspension of 120 g of the 4-methylsulfonylphenylacetyl chloride obtained above in 200 ml of fluorobenzene at a temperature of 0° to 3° C. The reaction vessel used was rinsed with 30 ml of fluorobenzene and the mixture was stirred at 20° C. for 4 hours. The reaction mixture was gradually poured into a mixture of ice water and hydrochloric acid and left to stand overnight, giving gummy solids. The solids were collected by filtration. The organic layer was separated from the filtrate and subjected to distillation under reduced pressure to recover 200 ml (52%) of fluorobenzene. The gummy solids were dissolved in dichloromethane, washed sequentially with water, a 5% aqueous solution of sodium bicarbonate and a saturated saline solution and dried over magnesium sulfate. The dichloromethane was distilled off and the resulting crystals were washed with diethyl ether, giving 77 g (51%) of 1-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)ethanone as pale yellow solids. To the suspension was added dropwise The reaction vessel used was rinsed with 30 ml of fluorobenzene The reaction mixture was gradually poured into a mixture of ice water and hydrochloric acid left to stand overnight giving gummy solids The solids were collected by filtration The organic layer was separated from the filtrate subjected to distillation under reduced pressure to recover 200 ml (52%) of fluorobenzene The gummy solids were dissolved in dichloromethane washed sequentially with water a 5% aqueous solution of sodium bicarbonate and a saturated saline solution and dried over magnesium sulfate The dichloromethane was distilled off the resulting crystals were washed with diethyl ether

反应条件: temp:90.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: First, a mixture of 110 g (0.51 mole) of 4-methylsulfonylphenylacetic acid and 110 ml (1.51 moles) of thionyl chloride was heated at 90° C. for 2 hours. After completion of the reaction, an excess of thionyl chloride was distilled off under reduced pressure, giving about 120 g of 4-methylsulfonylphenylacetyl chloride as a light brown solid. The solid thus obtained was subjected to the subsequent reaction without isolation and purification. After completion of the reaction an excess of thionyl chloride was distilled off under reduced pressure