1-(3-chlorophenyl)-3-(1,3-dioxolan-2-yl)propan-1-one

Conditions: temp:23.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 2-(2-Bromoethyl)-1,3-dioxolane (40 ml) was added dropwise within 15 minutes under argon and while stirring at a maximum 30° C. to a suspension of Rieke magnesium, prepared from 44.9 g of magnesium chloride, in 1500 ml of absolute tetrahydrofuran. The suspension was stirred at room temperature (about 23° C.) for 15 minutes, cooled to 0° C. and, after the addition of 43.5 g of copper(I) bromide, stirred at 5° C. for 15 minutes. After cooling to -70° C. 33 ml of 3-chlorobenzoyl chloride were added dropwise within 10 minutes. The reaction mixture was stirred at -70° C. for 15 minutes and at room temperature for 2 hours and subsequently hydrolyzed with 1000 ml of saturated ammonium chloride solution while cooling at a maximum 20° C. After the addition of 500 ml of water the mixture was extracted three times with 1000 ml of ethyl acetate each time. The combined organic extracts were washed with 1000 ml of saturated sodium chloride solution, dried over MgSO4 and freed from solvent. 59.2 g of oil were chromatographed on 1500 g of silica gel with ethyl acetate/hexane (1:3) as the eluent. 20.9 g (34%) of 3'-chloro-3-(1,3-dioxolan-2-yl)propiophenone were isolated as a yellow oil. cooled to 0° C. stirred at 5° C. for 15 minutes After cooling to -70° C while cooling at a maximum 20° C was extracted three times with 1000 ml of ethyl acetate each time The combined organic extracts were washed with 1000 ml of saturated sodium chloride solution dried over MgSO4 59.2 g of oil were chromatographed on 1500 g of silica gel with ethyl acetate/hexane (1:3) as the eluent

Conditions: temp:23.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 2-(2-Bromoethyl)-1,3-dioxolane (40 ml) was added dropwise within 15 minutes under argon and while stirring at a maximum 30° C. to a suspension of Rieke magnesium, prepared from 44.9 g of magnesium chloride, in 1500 ml of absolute tetrahydrofuran. The suspension was stirred at room temperature (about 23° C.) for 15 minutes, cooled to 0° C. and, after the addition of 43.5 g of copper(I) bromide, stirred at 5° C. for 15 minutes. After cooling to -70° C. 33 ml of 3-chlorobenzoyl chloride were added dropwise within 10 minutes. The reaction mixture was stirred at -70° C. for 15 minutes and at room temperature for 2 hours and subsequently hydrolyzed with 1000 ml of saturated ammonium chloride solution while cooling at a maximum 20° C. After the addition of 500 ml of water the mixture was extracted three times with 1000 ml of ethyl acetate each time. The combined organic extracts were washed with 1000 ml of saturated sodium chloride solution, dried over MgSO4 and freed from solvent. 59.2 g of oil were chromatographed on 1500 g of silica gel with ethyl acetate/hexane (1:3) as the eluent. 20.9 g (34%) of 3'-chloro-3-(1,3-dioxolan-2-yl)propiophenone were isolated as a yellow oil. cooled to 0° C. stirred at 5° C. for 15 minutes After cooling to -70° C while cooling at a maximum 20° C was extracted three times with 1000 ml of ethyl acetate each time The combined organic extracts were washed with 1000 ml of saturated sodium chloride solution dried over MgSO4 59.2 g of oil were chromatographed on 1500 g of silica gel with ethyl acetate/hexane (1:3) as the eluent

Conditions: temp:23.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 2-(2-Bromoethyl)-1,3-dioxolane (40 ml) was added dropwise within 15 minutes under argon and while stirring at a maximum 30° C. to a suspension of Rieke magnesium, prepared from 44.9 g of magnesium chloride, in 1500 ml of absolute tetrahydrofuran. The suspension was stirred at room temperature (about 23° C.) for 15 minutes, cooled to 0° C. and, after the addition of 43.5 g of copper(I) bromide, stirred at 5° C. for 15 minutes. After cooling to -70° C. 33 ml of 3-chlorobenzoyl chloride were added dropwise within 10 minutes. The reaction mixture was stirred at -70° C. for 15 minutes and at room temperature for 2 hours and subsequently hydrolyzed with 1000 ml of saturated ammonium chloride solution while cooling at a maximum 20° C. After the addition of 500 ml of water the mixture was extracted three times with 1000 ml of ethyl acetate each time. The combined organic extracts were washed with 1000 ml of saturated sodium chloride solution, dried over MgSO4 and freed from solvent. 59.2 g of oil were chromatographed on 1500 g of silica gel with ethyl acetate/hexane (1:3) as the eluent. 20.9 g (34%) of 3'-chloro-3-(1,3-dioxolan-2-yl)propiophenone were isolated as a yellow oil. cooled to 0° C. stirred at 5° C. for 15 minutes After cooling to -70° C while cooling at a maximum 20° C was extracted three times with 1000 ml of ethyl acetate each time The combined organic extracts were washed with 1000 ml of saturated sodium chloride solution dried over MgSO4 59.2 g of oil were chromatographed on 1500 g of silica gel with ethyl acetate/hexane (1:3) as the eluent