HRID8141

反应详情

EQUATION

反应方程式

HRID 8141 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

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.

WORKUP

后处理

  1. customof degassed 4:1 H2O/MeOH
  2. temperatureOn cooling to RT
  3. customthe organic phase was separated
  4. washwashed with 3×25 mL of Et2O
  5. washThe combined organic extracts were washed with 3×25 mL of H2O and 1×20 mL of brine
  6. dry with materialdried over Na2SO4
  7. customAfter removing the volatiles in vacuo
  8. customthe resultant brown oil was chromatographed on silica with 0–50% hexanes/CH2Cl2
  9. customthe volatiles were removed
  10. customto provide 2-formyl-6-naphthlypyridine as a white solid