تفاعل #977780

ord-4349d3c002cf48ecaa7f1be376d1a371

معادلة التفاعل

[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

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe volatiles were evaporated
  2. 2
    workup.DISSOLUTIONthe resulting oil was dissolved in dichloromethane (100 mL)
  3. 3
    أخرىwere separated
  4. 4
    استخلاصthe aqueous layer was extracted with dichloromethane (3×50 mL)
  5. 5
    غسيلThe combined organic layers were washed with water (50 mL) and brine (50 mL)
  6. 6
    تجفيفwas dried over MgSO4
  7. 7
    أخرىEvaporation of the solvent

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06998405B2uspto-grants-2006_02