反応 #2267067

ord-89d1ca474eec4fffb08f3ac65fa0eff7

反応方程式

COc1cccc(CC(C)=O)c1
3-methoxyphenylacetone
[BH4-].[Na+]
NaBH4
COc1cccc(CC(C)O)c1
desired product 2
収率 100.0%
COc1cccc(CC(C)O)c1
1-(3-Methoxyphenyl)-2-propyl alcohol
収率 100.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出It was extracted with CHCl3 three times
  2. 2
    洗浄The combined organic phase was washed with brine
  3. 3
    乾燥dried over Na2SO4
  4. 4
    その他Removal of the solvent
  5. 5
    その他afforded the crude product
  6. 6
    その他Purification of the crude product

実験手順

To a solution of 3-methoxyphenylacetone (1, 1.0 g) in methanol (30 ml) was added NaBH4 (360 mg) in portions in the period of 20 min at 0° C. The resulting solution was stirred at such temperature for another 40 min. No more starting materials were detected from TLC. Ice water was added to the reaction slowly. It was extracted with CHCl3 three times. The combined organic phase was washed with brine, and dried over Na2SO4. Removal of the solvent afforded the crude product. Purification of the crude product by using a silica gel column gave the desired product 2 (1.01 g, 100%).

出典

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