反应 #2348128

反应方程式

H2O

3-amino-4-[(E)-2-(4-hydroxy-phenyl)vinyl]phenol

acetic anhydride

Et3N

→

N-{5-hydroxy-2-[(E)-2-(4-hydroxyphenyl)vinyl]phenyl}-acetamide

收率 46.4%

溶剂

methanol

THF

反应条件

后处理

1. 1
   浓缩The reaction mixture was concentrated by vacuum evaporation
2. 2
   其他was not further purified
3. 3
   其他The crude mixture from the previous reaction
4. 4
   workup.STIRRINGThe resulting solution was vigorously stirred at rt for 1 h
5. 5
   其他All volatile solvents were evaporated

实验过程

To the solution of 3-amino-4-[(E)-2-(4-hydroxy-phenyl)vinyl]phenol (100 mg) in anhydrous THF was added 225 mg of acetic anhydride and 223 mg of Et3N. The resulting solution was stirred at rt overnight. The reaction mixture was concentrated by vacuum evaporation. The residue, which was identified as mainly desired compound by 1H-NMR, was not further purified and used directly for the next step. The crude mixture from the previous reaction was dissolved in 30 mL of methanol. K2Co3 (197 mg, ˜12 eq.) was added as well as 20 mL of H2O. The resulting solution was vigorously stirred at rt for 1 h. All volatile solvents were evaporated and the residue was loaded on a silica gel column with 5% MeOH/dichloromethane as eluent to give N-{5-hydroxy-2-[(E)-2-(4-hydroxyphenyl)vinyl]phenyl}-acetamide (55 mg, 46.4% in two steps). MS (ES) m/z: 270.14 (M+1); Mp. 227-229° C.

来源