HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71074Generated: October 26, 2026
Potassium Carbonate → 2-Chloro-6-(3-methoxyphenyl)pyridine
https://huagongshe.com/reaction/71074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,6-Dichloropyridine | HCID 16989 | — |
| Reactant | (3-Methoxyphenyl)boronic acid | HCID 2734370 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Chloro-6-(3-methoxyphenyl)pyridine | HCID 59489304 | — |
Reaction Steps
A mixture of m-methoxy-phenylboronic acid (10 g, 65.8 mmol), 2,6-dichloropyridine (9.7 g, 65.8 mmol), potassium carbonate (27.3 g, 197.4 mmol), triphenylphosphine (2.07 g, 7.9 mmol), dimethoxyethane 250 mL and water 80 mL was prepared. Nitrogen was bubbled directly in the mixture for 20 minutes. Then palladium acetate was added (0.44 g, 2.0 mmol). Nitrogen was bubbled again in the mixture for another 10 minutes. The mixture was heated to reflux under nitrogen overnight. The reaction mixture was cooled to room temperature. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic layers were dried over magnesium sulfate, filtered and evaporated. The mixture was purified by silica column with up to 10% ethyl acetate in hexanes to gain 6.5 g colorless oil (45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822708B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-14f5509b1a96459b987abe0328b41779 |
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| Source note | uspto-grants-2014_09 |
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