HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227114Generated: October 27, 2026
Sodium Carbonate → 5-Bromo-2-(4-octylphenyl)pyridine
https://huagongshe.com/reaction/2227114
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,3-Dibromopyridine | HCID 817102 | — |
| Reactant | (4-octylphenyl)boronic Acid | HCID 4197992 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Bromo-2-(4-octylphenyl)pyridine | HCID 18471820 | 95% |
Reaction Steps
To a 1000 mL round bottom flask equipped with a stirbar was added dibromopyridine 7C (22.506 g), boronic acid 7B (22.356 g), tetrakis(triphenylphosphine)palladium(0) (3.294 g), saturated sodium carbonate solution (238 mL), and toluene (190 mL). A reflux condenser was attached and the reaction was heated at 100° C. for 24 hours. The cooled reaction mixture was extracted with 1:1 hexane:ethyl acetate, and the combined organic layers were washed with brine and dried over magnesium sulfate and the solvent was removed in vacuo. The solid product was dissolved in dichloromethane, placed on silica gel, and silica gel filtered. The elution solvents were hexane, which removed a higher Rf side product, and 2.5% E/H, resulting in 31.251 g of solid. The product was recrystallized from acetonitrile to give 30.125 g of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413448B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-084f9497f27543ada529675940335893 |
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| Source note | uspto-grants-2002_07 |
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