反応 #595345
ord-6106c76da08c493da1bebffda33bcfaf
反応方程式
溶媒
反応条件
後処理
- 1その他The solvent is then removed on a rotary evaporator
- 2洗浄washed once with 5 ml of water
- 3乾燥The organic phase is dried over magnesium sulfate
- 4その他the solvent is removed on a rotary evaporator
- 5ろ過filtered off
- 6その他It is then recrystallized from about 10 ml of methanol
- 7その他This gives needle-shaped crystals which are dried in a drying cabinet at 50° C
- 8その他A further product fraction is obtained by reprecipitation
- 9その他after recrystallization
実験手順
1.40 g (8.00 mmol) of 4-chlorobenzoyl chloride, 1.00 g (10.09 mmol) of methyl isocyanatoacetate and 5.9 ml (42.39 mmol) of triethylamine are dissolved in 15 ml of dry THF and stirred at RT for 48 h. The solvent is then removed on a rotary evaporator. The residue is taken up in 20 ml of ethyl acetate and washed once with 5 ml of water. The organic phase is dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The residue is suspended in 10 ml of cyclohexane and filtered off. It is then recrystallized from about 10 ml of methanol. This gives needle-shaped crystals which are dried in a drying cabinet at 50° C. A further product fraction is obtained by reprecipitation after recrystallization.