تفاعل #8237
ord-ff4c7be6474a4df4bc8cc7292c566b1d
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىof degassed 4:1 H2O/MeOH
- 2درجة الحرارةOn cooling to RT
- 3أخرىthe organic phase was separated
- 4غسيلwashed with 3×25 mL of Et2O
- 5غسيلThe combined organic extracts were washed with 3×25 mL of H2O and 1×20 mL of brine
- 6تجفيفdried over Na2SO4
- 7أخرىAfter removing the volatiles in vacuo
- 8أخرىthe resultant brown oil was chromatographed on silica with 0–50% hexanes/CH2Cl2
- 9أخرىthe volatiles were removed
- 10أخرىto provide 2-formyl-6-naphthlypyridine as a white solid
الإجراء التجريبي
Naphthylboronic acid (2.06 g, 12 mmol) and Na2CO3 (2.65 g, 25 mmol) were dissolved in 60 mL of degassed 4:1 H2O/MeOH. This solution was added via cannula to a solution of 1.86 g (10 mmol) of 2-bromo-6-formylpyridine and I 16 mg (0.10 mmol) of Pd(PPh3)4 in 50 mL of degassed toluene. The biphasic solution was vigorously stirred and heated to 70° C. under N2 for 4 h. On cooling to RT, the organic phase was separated and washed with 3×25 mL of Et2O. The combined organic extracts were washed with 3×25 mL of H2O and 1×20 mL of brine and dried over Na2SO4. After removing the volatiles in vacuo, the resultant brown oil was chromatographed on silica with 0–50% hexanes/CH2Cl2. The early fractions contained naphthalene and binaphthyl and were discarded. The remaining fractions were combined and the volatiles were removed to provide 2-formyl-6-naphthlypyridine as a white solid.