3-氯-N-甲基-丙酰胺

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

实验步骤: A mixture of 5.0 g (0.017 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 3.0 g (0.025 mole) of 3-chloro-N-methylpropanamide, 15.0 g (0.142 mole) of anhydrous sodium carbonate and 0.3 g (0.002 mole) of potassium iodide in 100 ml of N,N-dimethylformamide was heated on a steam bath for 16 h. The mixture was poured into 1.5 L of water and extracted twice with 150 ml portions of ethyl acetate. The ethyl acetate fractions were combined, washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to give a dark oil. The oil was purified by column chromatography using 150 g of silica gel on a 60 cm×3.5 cm column, eluted with 10% methanol in methylene chloride. The fractions containing the desired product were partitioned between 15% sodium hydroxide and methylene chloride. The methylene chloride layer was washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to give a glass. Upon trituration with petroleum ether (30°-60° C.), the glass solidified. The solid was recrystallized from ethyl acetate/petroleum ether (30°-60° C.) to yield 3.2 g (50%) of white solid, mp 127°-129° C. was heated on a steam bath for 16 h extracted twice with 150 ml portions of ethyl acetate washed with water and brine dried (MgSO4) concentrated under reduced pressure to give a dark oil The oil was purified by column chromatography eluted with 10% methanol in methylene chloride The fractions containing the desired product were partitioned between 15% sodium hydroxide and methylene chloride The methylene chloride layer was washed with water and brine dried (MgSO4) concentrated under reduced pressure to give a glass The solid was recrystallized from ethyl acetate/petroleum ether (30°-60° C.)

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

实验步骤: A mixture of 5.0 g (0.017 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 3.0 g (0.025 mole) of 3-chloro-N-methylpropanamide, 15.0 g (0.142 mole) of anhydrous sodium carbonate and 0.3 g (0.002 mole) of potassium iodide in 100 ml of N,N-dimethylformamide was heated on a steam bath for 16 h. The mixture was poured into 1.5 L of water and extracted twice with 150 ml portions of ethyl acetate. The ethyl acetate fractions were combined, washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to give a dark oil. The oil was purified by column chromatography using 150 g of silica gel on a 60 cm×3.5 cm column, eluted with 10% methanol in methylene chloride. The fractions containing the desired product were partitioned between 15% sodium hydroxide and methylene chloride. The methylene chloride layer was washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to give a glass. Upon trituration with petroleum ether (30°-60° C.), the glass solidified. The solid was recrystallized from ethyl acetate/petroleum ether (30°-60° C.) to yield 3.2 g (50%) of white solid, mp 127°-129° C. was heated on a steam bath for 16 h extracted twice with 150 ml portions of ethyl acetate washed with water and brine dried (MgSO4) concentrated under reduced pressure to give a dark oil The oil was purified by column chromatography eluted with 10% methanol in methylene chloride The fractions containing the desired product were partitioned between 15% sodium hydroxide and methylene chloride The methylene chloride layer was washed with water and brine dried (MgSO4) concentrated under reduced pressure to give a glass The solid was recrystallized from ethyl acetate/petroleum ether (30°-60° C.)

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

实验步骤: A mixture of 5.0 g (0.017 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 3.0 g (0.025 mole) of 3-chloro-N-methylpropanamide, 15.0 g (0.142 mole) of anhydrous sodium carbonate and 0.3 g (0.002 mole) of potassium iodide in 100 ml of N,N-dimethylformamide was heated on a steam bath for 16 h. The mixture was poured into 1.5 L of water and extracted twice with 150 ml portions of ethyl acetate. The ethyl acetate fractions were combined, washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to give a dark oil. The oil was purified by column chromatography using 150 g of silica gel on a 60 cm×3.5 cm column, eluted with 10% methanol in methylene chloride. The fractions containing the desired product were partitioned between 15% sodium hydroxide and methylene chloride. The methylene chloride layer was washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to give a glass. Upon trituration with petroleum ether (30°-60° C.), the glass solidified. The solid was recrystallized from ethyl acetate/petroleum ether (30°-60° C.) to yield 3.2 g (50%) of white solid, mp 127°-129° C. was heated on a steam bath for 16 h extracted twice with 150 ml portions of ethyl acetate washed with water and brine dried (MgSO4) concentrated under reduced pressure to give a dark oil The oil was purified by column chromatography eluted with 10% methanol in methylene chloride The fractions containing the desired product were partitioned between 15% sodium hydroxide and methylene chloride The methylene chloride layer was washed with water and brine dried (MgSO4) concentrated under reduced pressure to give a glass The solid was recrystallized from ethyl acetate/petroleum ether (30°-60° C.)