HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402056Generated: October 27, 2026
Sodium Carbonate → 2-Chloro-4-(5-chloro-2-methoxyphenyl)pyridine
https://huagongshe.com/reaction/1402056
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-Chloro-2-iodoanisole | HCID 2800978 | — |
| Reactant | 2-Chloropyridine-4-boronic acid | HCID 5151595 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-4-(5-chloro-2-methoxyphenyl)pyridine | HCID 59436473 | — |
Reaction Steps
A mixture of 4-chloro-2-iodo-1-methoxybenzene (542 mg, 2.02 mmol), (2-chloropyridin-4-yl)boronic acid (400 mg, 2 mmol), and sodium carbonate (860.2 mg, 8.116 mmol) in 1,4-dioxane (8.4 mL, 110 mmol) and water (2.8 mL, 160 mmol) was sparged 5 minutes with argon. Tetrakis(triphenylphosphine)palladium(0) (139.9 mg, 0.1210 mmol) was added and the reaction vial was capped. The reaction mixture was heated at 90° C. After 3 hours, the reaction mixture was cooled to ambient temperature and poured into water. The mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was taken up in methylene chloride, concentrated onto diatomaceous earth, and purified by automated flash chromatography (24 g SiO2, hexanes to 3:1 hexanes-ethyl acetate) to afford the product as a light yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907101B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-e8f26b4762ad4558b1c994ad862696bc |
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| Source note | uspto-grants-2014_12 |
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