تفاعل #8237

ord-ff4c7be6474a4df4bc8cc7292c566b1d

المذيبات

ظروف التفاعل

درجة الحرارة
70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىof degassed 4:1 H2O/MeOH
  2. 2
    درجة الحرارةOn cooling to RT
  3. 3
    أخرىthe organic phase was separated
  4. 4
    غسيلwashed with 3×25 mL of Et2O
  5. 5
    غسيلThe combined organic extracts were washed with 3×25 mL of H2O and 1×20 mL of brine
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    أخرىAfter removing the volatiles in vacuo
  8. 8
    أخرىthe resultant brown oil was chromatographed on silica with 0–50% hexanes/CH2Cl2
  9. 9
    أخرىthe volatiles were removed
  10. 10
    أخرىto 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087690B2uspto-grants-2006_08