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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963173Generated: October 30, 2026

Hydrochloric Acid → HCID 66731948, compound

https://huagongshe.com/reaction/1963173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-chloropyridine-4-carboxylateHCID 2736842—
Reactant(4-Chloro-2-fluorophenyl)boronic acidHCID 4193595—
CatalystPalladium ChlorideHCID 24290—
SolventMethanolHCID 887—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 66731948HCID 66731948102.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 2-chloroisonicotinate (4 g, 23.31 mmol), 4-chloro-2-fluorophenylboronic acid (6.10 g, 34.97 mmol), potassium carbonate (2.416 g, 17.48 mmol) and PdCl2 (dppf) (0.506 g, 0.70 mmol) were mixed in methanol (30 mL) in two separate 20 mL microwave vials. The vials were capped and heated at 100° C. for 10 min in a single node microwave reactor. Water and DCM were added and the phases were separated. The water phase (pH 9) was extracted with DCM and the combined organic phase washed with brine, passed through a phase separator and evaporated to yield a dark-orange solid. The solid was dissolved in MTBE and stirred for 15 minutes, then filtered. The orange MTBE layer was treated with hydrogen chloride (4 M in dioxane, 5.83 mL, 23.31 mmol) and stirred for 1 h at room temperature. The precipitate was collected by filtration to yield methyl 2-(4-chloro-2-fluorophenyl)isonicotinate hydrochloride (7.22 g, quant.) as a slightly orange solid. MS m/z 266 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-be9acddf06134ad9ad783bd93d97c9ce
Source noteuspto-grants-2013_04