反応 #1820503
ord-ba16d3c0cad2450fa4a5bbcb41b641a0
反応方程式
溶媒
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1温度cooling
- 2workup.STIRRINGstirred for two hours
- 3ろ過the resulting precipitate collected by suction filtration
- 4洗浄The filter cake is washed well with ether
- 5乾燥dried in vacuo at 40° C. over sodium hydroxide pellets
- 6ろ過The dried filter cake
- 7その他is recrystallized twice from a chloroform-ether mixture
実験手順
2.0 g of 1-methyl-4-(α-phenyl-2-tolyl)-4-piperidinol, Example 1, is treated with 10 ml of benzoyl chloride with stirring and cooling. The reaction solution is diluted with 20 ml of ether, stirred for two hours and the resulting precipitate collected by suction filtration. The filter cake is washed well with ether and dried in vacuo at 40° C. over sodium hydroxide pellets. The dried filter cake is recrystallized twice from a chloroform-ether mixture to give colorless crystals, mp 197°-198° C. of 4-benzoyloxy-1-methyl-4(α-phenyl-2-tolyl)piperidine hydrochloride.