反应 #1328408
ord-8531ec97041b4e96a1bc372c5203ea0c
反应方程式
反应物
试剂
溶剂
反应条件
后处理
- 1温度external cooling with an ice bath
- 2workup.STIRRINGStirring
- 3萃取extracted three times with 400 mL CH2Cl2 or EtOAc (the product
- 4过滤can be collected by filtration
- 5洗涤washed at this point, but it
- 6其他this results in a yield of only ˜60%)
- 7洗涤The combined organic extracts were washed with brine
- 8干燥dried with MgSO4
- 9其他evaporated
- 10其他The crude product was purified from the main byproduct
- 11workup.DISSOLUTIONby dissolving it in a minimum volume of CH2Cl2 or THF(˜175 ml)
- 12其他precipitating it by slowly adding hexane (1000 ml)
- 13workup.STIRRINGwhile stirring (yield 51 g; 80% overall)
- 14其他It can also be recrystallized (e.g., toluene-hexane)
实验过程
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 51 g; 80% overall). It can also be recrystallized (e.g., toluene-hexane), but this reduces the yield.