反応 #2348104
ord-bba72c164c9c42108512211edd5df851
反応方程式
反応物
試薬
溶媒
反応条件
後処理
- 1温度external cooling with an ice bath
- 2workup.STIRRINGStirring
- 3抽出extracted three times with 400 mL CH2Cl2 or EtOAc (the product
- 4ろ過can be collected by filtration
- 5洗浄washed at this point, but it
- 6その他this results in a yield of only ˜60%)
- 7洗浄The combined organic extracts were washed with brine
- 8乾燥dried with MgSO4
- 9その他evaporated
- 10その他The crude product was purified from the main byproduct
- 11workup.DISSOLUTIONby dissolving it in a minimum volume of CH2Cl2 or THF(˜175 ml)
- 12その他precipitating it by slowly adding hexane (1000 ml)
- 13workup.STIRRINGwhile stirring
- 14その他(yield Sig; 80% overall)
- 15その他It can also be recrystallized (e.g., toluene-hexane)
実験手順
Sodium borohydride (log; 0.27 mol) was added slowly to a cold, stirring suspension of 53 g (0.25 mol) of 4,5-methylenedioxy-2-nitroacetophenone in 400 mL methanol. The temperature was kept below 10° C. by slow addition of the NaBH4 and external cooling with an ice bath. Stirring was continued at ambient temperature for another two hours, at which time TLC (CH2Cl2) indicated complete conversion of the ketone. The mixture was poured into one liter of ice-water and the resulting suspension was neutralized with ammonium chloride and then extracted three times with 400 mL CH2Cl2 or EtOAc (the product can be collected by filtration and washed at this point, but it is somewhat soluble in water and this results in a yield of only ˜60%). The combined organic extracts were washed with brine, then dried with MgSO4 and evaporated. The crude product was purified from the main byproduct by dissolving it in a minimum volume of CH2Cl2 or THF(˜175 ml) and then precipitating it by slowly adding hexane (1000 ml) while stirring (yield Sig; 80% overall). It can also be recrystallized (e.g., toluene-hexane), but this reduces the yield.