反应 #586160

ord-ddae5143bdfa477abe9ddd8271d40b24

反应方程式

[BH4-].[Na+]
sodium borohydride
[BH4-].[Na+]
sodium borohydride
COc1ccc(C(=O)CC(=O)c2ccc(OC)cc2OC)c(OC)c1
1,3-Bis(2,4-dimethoxyphenyl)-propan-1,3-dione
CC(=O)O
acetic acid
COc1ccc(C(O)CC(O)c2ccc(OC)cc2OC)c(OC)c1
1,3-bis(2,4-dimethoxyphenyl)-propan-1,3-diol
COc1ccc(C(O)CC(O)c2ccc(OC)cc2OC)c(OC)c1
1,3-Bis(2,4-dimethoxyphenyl)-propan-1,3-diol

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 3 hours
  2. 2
    workup.ADDITIONwas added
  3. 3
    其他The mixture was then separated on a pre-packed C18 column
  4. 4
    洗涤eluting with a MeOH/H2O gradient

实验过程

1,3-Bis(2,4-dimethoxyphenyl)-propan-1,3-dione (8) (5 mg) was dissolved in 1-propanol (1 ml), followed by the addition of sodium borohydride (3 mg) and the mixture was allowed to react at room temperature for 3 hours. Upon completion of the reaction, 20% acetic acid (0.2 ml) was added to neutralize the excess sodium borohydride. The mixture was then separated on a pre-packed C18 column eluting with a MeOH/H2O gradient to provide 1,3-bis(2,4-dimethoxyphenyl)-propan-1,3-diol (9).

来源

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