HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46384Generated: October 26, 2026
Sodium Carbonate → 2-Chloro-4-(5-chloro-2-methoxyphenyl)pyridine
https://huagongshe.com/reaction/46384
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Chloro-2-iodoanisole | HCID 2800978 | — |
| Reactant | 2-Chloropyridine-4-boronic acid | HCID 5151595 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Chloro-4-(5-chloro-2-methoxyphenyl)pyridine | HCID 59436473 | — |
Reaction Steps
To a nitrogen purged aqueous solution of sodium carbonate (2M, 14 mL) and ethylene glycol dimethyl ether (25 mL) was added 4-chloro-2-iodoanisole (2.50 g, 0.00931 mol), 2-chloropyridine-4-boronic acid (1.61 g, 0.0102 mol) and bis(triphenylphosphine)palladium (II) dichloride (327 mg, 0.00047 mol). The reaction mixture was warmed to 50° C. and stirred for 5 hours. Following LCMS analysis the reaction was warmed to 75° C. and stirred for 5 hours before cooling to room temperature. The reaction was partitioned between ethyl acetate (100 mL) and a 10% w/v aqueous solution of citric acid (50 mL). The organic layer was washed with water (50 mL), dried over anhydrous magnesium sulphate, filtered and the solvents removed in vacuo to give the crude product as an orange oil (2.95 g). The material was purified using an ISCO™ companion (120 g column, eluting with 100% heptane to 7:3 heptane/ethyl acetate). Fractions containing product were combined and concentrated in vacuo to obtain the title compound as an off white solid (1.10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541588B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-79ae207cb7e44c648369753e2f7fe8dd |
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| Source note | uspto-grants-2013_09 |
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