一甲胺 → N-(4-甲氧基苄基)-N-甲胺

HRID 347796

反应方程式

HRID 347796 反应方程式
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.[CH3:11][NH2:12].[BH4-].[Na+]>C(O)C>[CH3:11][NH:12][CH2:7][C:6]1[CH:9]=[CH:10][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1

参与物

5

实验过程

A mixture of p-methoxybenzaldehyde (25 ml; 200 mmol) and 8M methylamine in ethanol (100 ml; 800 mmol) in 100 ml of ethanol was stirred at rt for 18 hours. After removing the volatiles in vacuo, the residue was dissolved in 300 ml of fresh ethanol and sodium borohydride (8.5 g; 225 mmol) was added portionwise over 1.5 hr. Following the addition, the reaction mixture was concentrated to ˜⅓ volume and water (50 ml) was added. After cooling in an ice bath, the stirred mixture was carefully acidified to pH ˜2 with 5% aqueous H2SO4. After stirring 15 minutes, the mixture was basified to pH 14 with 6N NaOH and extracted with ethyl ether (400 ml). The ether layer was washed with water (200 ml), brine (100 ml) and dried over MgSO4. Concentration afforded 28.04 g (93%) of B51.1 as a colorless liquid. (M+H)+=152.13 (HPLC>94%).

后处理

  1. customAfter removing the volatiles in vacuo
  2. dissolutionthe residue was dissolved in 300 ml of fresh ethanol
  3. additionthe addition
  4. concentrationthe reaction mixture was concentrated
  5. additionwas added
  6. temperatureAfter cooling in an ice bath
  7. stirringAfter stirring 15 minutes
  8. extractionextracted with ethyl ether (400 ml)
  9. washThe ether layer was washed with water (200 ml), brine (100 ml)
  10. dry with materialdried over MgSO4
  11. concentrationConcentration
  12. customafforded 28.04 g (93%) of B51.1 as a colorless liquid

来源与证据

ORD记录
ord-951d120e73cb4074bdc7c86d69986e09
来源数据集
uspto-grants-2007_02
专利号
US07176214B2

关联笔记

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