Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassium FluorideHCID 522689—
Reactant2,6-Difluoro-4-methoxybenzeneboronic acidHCID 16217424—
ReactantMethyl 6-bromo-5-fluoropyridine-2-carboxylateHCID 46311204—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 6-(2,6-difluoro-4-methoxyphenyl)-5-fluoropicolinateHCID 5922646085%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173883B2
Source datasetuspto-grants-2015_11
ORD IDord-f12289236517459faab528343748fba3
Source noteuspto-grants-2015_11