Réaction #1747829

ord-a2b3314375b34ca899e1ebdbddc89a72

Équation de réaction

[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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe volatiles were evaporated
  2. 2
    workup.DISSOLUTIONthe resulting oil was dissolved in dichloromethane (100 mL)
  3. 3
    Autrewere separated
  4. 4
    Extractionthe aqueous layer was extracted with dichloromethane (3×50 mL)
  5. 5
    LavageThe combined organic layers were washed with water (50 mL) and brine (50 mL)
  6. 6
    Séchagewas dried over MgSO4
  7. 7
    AutreEvaporation of the solvent

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE042802E1uspto-grants-2011_10