反应 #1747829

ord-a2b3314375b34ca899e1ebdbddc89a72

反应方程式

[Na+].[OH-]
NaOH
CCCN
n-propylamine
COc1ccc(CCC(=O)O)cc1
3-(4-methoxyphenyl)-propionic acid
O=S(Cl)Cl
thionylchloride
CCCNC(=O)CCc1ccc(OC)cc1
amide
CCCNC(=O)CCc1ccc(OC)cc1
3-(4-methoxyphenyl)-propionic acid n-propylamide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The volatiles were evaporated
  2. 2
    workup.DISSOLUTIONthe resulting oil was dissolved in dichloromethane (100 mL)
  3. 3
    其他were separated
  4. 4
    萃取the aqueous layer was extracted with dichloromethane (3×50 mL)
  5. 5
    洗涤The combined organic layers were washed with water (50 mL) and brine (50 mL)
  6. 6
    干燥was dried over MgSO4
  7. 7
    其他Evaporation of the solvent

实验过程

3-(4-methoxyphenyl)-propionic acid (8.8 g, 49 mmol) was refluxed in dichloromethane (200 mL) with thionylchloride (6.6 mL, 90 mmol) for 1 h. The volatiles were evaporated and the resulting oil was dissolved in dichloromethane (100 mL). This was added to a vigorously stirred mixture of 5% aqueous NaOH (200 mL), dichloromethane (100 mL) and n-propylamine (3.0 mL, 71 mmol). After stirring for 1 h the layers were separated and the aqueous layer was extracted with dichloromethane (3×50 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL) and was dried over MgSO4. Evaporation of the solvent gave the amide in quantitative yield (10.7 g, 49 mmol, 100%). IR (neat) cm−1 3300, 2961; 1734, 1642; MS (EI) m/z 221 (M+) Analyses were in agreement with literature data.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE042802E1uspto-grants-2011_10