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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8141Generated: October 26, 2026

Sodium Carbonate → 2-Formyl-6-naphthylpyridine

https://huagongshe.com/reaction/8141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Naphthaleneboronic acidHCID 254532—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-Formyl-6-naphthylpyridineHCID 12070561—

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087690B2
Source datasetuspto-grants-2006_08
ORD IDord-ff4c7be6474a4df4bc8cc7292c566b1d
Source noteuspto-grants-2006_08