HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705183Generated: October 26, 2026
Tris(1,1-dimethylethyl)phosphine → Methyl 6-(2,6-difluoro-4-methoxyphenyl)-5-fluoropicolinate
https://huagongshe.com/reaction/705183
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2,6-Difluoro-4-methoxybenzeneboronic acid | HCID 16217424 | — |
| Reactant | Methyl 6-bromo-5-fluoropyridine-2-carboxylate | HCID 46311204 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 6-(2,6-difluoro-4-methoxyphenyl)-5-fluoropicolinate | HCID 59226460 | 85% |
Reaction Steps
To a solution of methyl 6-bromo-5-fluoropicolinate (1.0 equiv.) in THF and water (10:1, 0.1 M) was added 2,6-difluoro-4-methoxyphenylboronic acid (2.5 equiv.) and potassium fluoride (3.3 equiv.). The reaction was degassed with nitrogen, then Pd2(dba)3 (0.25 equiv.) and tri-tert-butylphosphine (0.5 equiv.) were added and the reaction was heated to 80° C. for one hour. LC/MS analysis indicated complete conversion of the starting material to product. The reaction was cooled to room temperature, then concentrated in vacuo and fused to silica gel. The crude product was purified by ISCO flash chromatography eluting with ethyl acetate and hexanes (0% to 30% ethyl acetate) to provide methyl 6-(2,6-difluoro-4-methoxyphenyl)-5-fluoropicolinate as a white solid in 85% yield. LC/MS=298.0 (M+H), Rt=0.89 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09173883B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-f12289236517459faab528343748fba3 |
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| Source note | uspto-grants-2015_11 |
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