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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717814Generated: October 26, 2026

Potassium Carbonate → Methyl 5-chloro-2-(3-fluorophenyl)nicotinate

https://huagongshe.com/reaction/717814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluorophenylboronic acidHCID 2733986—
ReactantMethyl 2,5-DichloronicotinateHCID 2764318—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 5-chloro-2-(3-fluorophenyl)nicotinateHCID 5851598383%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of methyl 2,5-dichloronicotinate (8.2 g, 40 mmol), (3-fluorophenyl)boronic acid (6.1 g, 44 mmol), and potassium carbonate (12 g, 86 mmol) in water (71 mL) and 1,4-dioxane (190 mL) was degassed with nitrogen (10 minutes). The reaction mixture was treated with bis(triphenylphosphine)palladium(II) chloride (3.1 g, 4.4 mmol), degassed with nitrogen (10 minutes), and heated at 80° C. for 14.5 hours. The reaction mixture was diluted with ethyl acetate and water and filtered over celite. The aqueous layer was separated and re-extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried with magnesium sulfate, filtered, and concentrated to a crude residue. Purification by flash column chromatography using ethyl acetate in hexanes (0-80%) gave the desired product (8.7 g, 83%). LCMS calculated for C13H10ClFNO2 (M+H)+: m/z=266.0. found: 265.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193721B2
Source datasetuspto-grants-2015_11
ORD IDord-26d8ebe933b34a42bcd68ba333d6a270
Source noteuspto-grants-2015_11