Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407226Generated: October 26, 2026

1,10-Phenanthroline → HCID 86675407, compound

https://huagongshe.com/reaction/407226

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 4-amino-6-chloro-5-fluoro-3-iodopicolinateHCID 86668303—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventMethanolHCID 887—
ProductHCID 86675407HCID 86675407—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a dry 1 liter (L) flask was added methyl 4-amino-6-chloro-5-fluoro-3-iodopicolinate (50 g, 151 mmol) and cesium carbonate (Cs2CO3; 99 g, 303 mmol). CH3OH (378 mL) was added, and the solution was sparged with nitrogen for 10 min. 1,10-Phenanthroline (6.00 g, 30.3 mmol) and copper(I) iodide (CuI; 2.88 g, 15.13 mmol) were added, and the flask was fitted with a reflux condenser and heated to 65° C. under nitrogen. After 12 h, CuI (2.88 g, 15.13 mmol) was again added to the reaction mixture, and heating was continued until consumption of the iodopicolinate was observed. The reaction mixture was cooled to room temperature, filtered through Celite, and concentrated in vacuo. To the crude residue was added EtOAc (100 mL) and H2O (100 mL). The layers were separated, and the aqueous phase was acidified to pH=2 with concentrated (conc) HCl and subsequently extracted with EtOAc (3×100 mL). The organic extracts were combined, washed with satd aq NaCl, dried (Na2SO4), filtered, and concentrated in vacuo to afford 4-amino-6-chloro-5-fluoro-3-methoxypicolinic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754229B2
Source datasetuspto-grants-2014_06
ORD IDord-bd8262ffb7544558a1518fe2228aec94
Source noteuspto-grants-2014_06