تفاعل #2460294
ord-b63701f36ce544c08f35518751e28df6
معادلة التفاعل
الكواشف
المذيبات
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المعالجة
- 1أخرىFirst, 2-[(3-methoxyphenyl)thio]benzoic acid was prepared
- 2درجة الحرارةwas heated
- 3درجة الحرارةat reflux for 2 h
- 4درجة الحرارةcooled
- 5غسيلwashed twice with 10% aqueous HCl
- 6تجفيفdried (Na2SO4)
- 7أخرىThe solvent is removed at reduced pressure
- 8أخرىThe product was purified by recrystallization from heptane
الإجراء التجريبي
First, 2-[(3-methoxyphenyl)thio]benzoic acid was prepared. A mixture of thiosalicylic acid (1.5 g, 9.7 mmol), 3-methoxyiodobenzene (4.6 g, 19.4 mmol), copper (I) iodide (0.07 g, 0.4 mmol), potassium carbonate (4.0 g, 29.2 mmol), and N,N-dimethylformamide (25 mL) was heated at reflux for 2 h and then cooled to ambient. The reaction mixture was diluted with ether, washed twice with 10% aqueous HCl, and dried (Na2SO4). The solvent is removed at reduced pressure to deposit a brown solid. The product was purified by recrystallization from heptane to provide 1.0 g (40% of theory) of 2-[(3-methoxyphenyl)thio]benzoic acid as a tan solid. 1H NMR (CDCl3): δ 3.80 (s, 3H), 6.90 (d, 1H), 7.00 (d, 1H), 7.25 (m, 5H), 8.11 (d, 1H).