反応 #2267069

ord-707090167f8a43f1941721a79a3024ae

反応方程式

COc1ccc2c(c1)CC(C)OC2c1ccc([N+](=O)[O-])cc1
3
COc1ccc2c(c1)CC(C)OC2c1ccc([N+](=O)[O-])cc1
3-Methyl-1-(4-nitrophenyl)-6-methoxyisochroman
[Na+].[OH-]
sodium hydroxide
Cl
HCl
COc1ccc2c(c1)CC(C)OC2(O)c1ccc([N+](=O)[O-])cc1
crude product
COc1ccc2c(c1)CC(C)OC2(O)c1ccc([N+](=O)[O-])cc1
1-Hydroxy-3-methyl-1-(4-nitrophenyl)-6-methoxyisochroman

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted with ethyl acetate three times
  2. 2
    洗浄The combined organic phase was washed with water in order
  3. 3
    その他to remove DMF
  4. 4
    乾燥dried over Na2SO4
  5. 5
    その他Removal of the solvent

実験手順

A solution of 3 (1.3 g) in 4 ml of DMSO and 24 ml of DMF was cooled to 8-12° C. and air was passed through the mixture. To the solution was added 1.2 ml of 50% aqueous sodium hydroxide in one portion and the resulting mixture was stirred for 5 hours. HCl (1 N) was added, and extracted with ethyl acetate three times. The combined organic phase was washed with water in order to remove DMF, dried over Na2SO4. Removal of the solvent afforded syrup crude product (1.6 g), which was used directly for the next step.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06887867B2uspto-grants-2005_05