反应 #586159

ord-8882ef8d2b444ebeaf698a1c0823f539

反应方程式

[BH4-].[Na+]
sodium borohydride
[BH4-].[Na+]
sodium borohydride
COc1ccc(CCC(=O)c2cc(OC)ccc2O)c(OC)c1
1-(2-hydroxy-5-methoxyphenyl)-3-(2′,4′-dimethoxyphenyl)-1-propanone
CC(=O)O
acetic acid
COc1ccc(CCC(O)c2cc(OC)ccc2O)c(OC)c1
1-(2-hydroxy-5-methoxyphenyl)-3-(2′,4′-dimethoxyphenyl)-1-propanol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他to react at room temperature for 5 hours
  2. 2
    workup.ADDITIONwas added
  3. 3
    其他The reaction mixture was then separated on a pre-packed C18 column
  4. 4
    洗涤eluting with a MeOH/H2O gradient

实验过程

1-(2-hydroxy-5-methoxyphenyl)-3-(2′,4′-dimethoxyphenyl)-1-propanone (6) (5 mg) was dissolved in 1-propanol (1 ml), followed by the addition of sodium borohydride (2 mg) and the mixture was allowed to react at room temperature for 5 hours. Upon completion of the reaction, 20% acetic acid (0.2 ml) was added to neutralize the excess sodium borohydride. The reaction mixture was then separated on a pre-packed C18 column eluting with a MeOH/H2O gradient to provide 1-(2-hydroxy-5-methoxyphenyl)-3-(2′,4′-dimethoxyphenyl)-1-propanol (7).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07767661B2uspto-grants-2010_08