Réaction #2460292

Équation de réaction

2-chlorobenzoic acid

4-butoxyphenol

potassium carbonate

HCl

→

2-(4-butoxyphenoxy)benzoic acid

Rendement 45.1%

Solvants

N,N-dimethylformamide

Conditions de réaction

Traitement

1. 1
   AutreFirst, 2-(4-butoxyphenoxy)benzoic acid was prepared
2. 2
   Températurewas heated
3. 3
   Températureat reflux for 5 h
4. 4
   Températurecooled
5. 5
   ExtractionThe precipitated product was extracted into diethyl ether
6. 6
   AutreThe product was purified by extraction into 5% aqueous NaOH
7. 7
   AutreThe precipitate was collected
8. 8
   Lavagewashed with water
9. 9
   Séchagedried in vacuo over CaSO4

Mode opératoire

First, 2-(4-butoxyphenoxy)benzoic acid was prepared. A stirred mixture of 2-chlorobenzoic acid (10.0 g, 64 mmol), 4-butoxyphenol (12.7 g, 77 mmol), potassium carbonate (17.6 g, 128 mmol), copper powder (0.24 g, 3.8 mmol), copper (I) iodide (0.20 g, 1.3 mmol), dithioerithritol (0.20 g, 1.3 mmol), and 75 mL of N,N-dimethylformamide was heated at reflux for 5 h and then cooled to ambient. The reaction mixture was poured onto a mixture of 300 g of ice plus 100 mL of 10% aqueous HCl. The precipitated product was extracted into diethyl ether. The product was purified by extraction into 5% aqueous NaOH, followed by acidification with concentrated HCl. The precipitate was collected, washed with water, and dried in vacuo over CaSO4 to provide 8.27 g (45% of theory) of 2-(4-butoxyphenoxy)benzoic acid as a brown powder.

Source