反应 #1328408

ord-8531ec97041b4e96a1bc372c5203ea0c

反应方程式

[BH4-].[Na+]
Sodium borohydride
CC(=O)c1cc2c(cc1[N+](=O)[O-])OCO2
4,5-methylenedioxy-2-nitroacetophenone
[BH4-].[Na+]
NaBH4
ClCCl
CH2Cl2
[Cl-].[NH4+]
ammonium chloride
CC(O)c1cc2c(cc1[N+](=O)[O-])OCO2
1-(4,5-Methylenedioxy-2-nitrophenyl) ethanol

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度external cooling with an ice bath
  2. 2
    workup.STIRRINGStirring
  3. 3
    萃取extracted three times with 400 mL CH2Cl2 or EtOAc (the product
  4. 4
    过滤can be collected by filtration
  5. 5
    洗涤washed at this point, but it
  6. 6
    其他this results in a yield of only ˜60%)
  7. 7
    洗涤The combined organic extracts were washed with brine
  8. 8
    干燥dried with MgSO4
  9. 9
    其他evaporated
  10. 10
    其他The crude product was purified from the main byproduct
  11. 11
    workup.DISSOLUTIONby dissolving it in a minimum volume of CH2Cl2 or THF(˜175 ml)
  12. 12
    其他precipitating it by slowly adding hexane (1000 ml)
  13. 13
    workup.STIRRINGwhile stirring (yield 51 g; 80% overall)
  14. 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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07115364B1uspto-grants-2006_10