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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480037Generated: October 27, 2026

Hydrochloric Acid → 5-Chloro-4-(3-chlorophenyl)-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1480037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant5-Chloro-4-iodo-2-pyridinecarboxylic acidHCID 85592091—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Chloro-4-(3-chlorophenyl)-pyridine-2-carboxylic acidHCID 90203766—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5-chloro-4-iodo-pyridine-2-carboxylic acid (CAN 120643-06-3, 500 mg, 1.76 mmol) in toluene (10 mL) was added with stirring the [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium DCM complex (144 mg, 0.176 mmol), B-(3-chlorophenyl)-boronic acid (552 mg, 3.53 mmol) and sodium carbonate (467 mg, 4.41 mmol) in water (3 mL). The resulting mixture was stirred at 80° C. for 23 h, cooled, poured onto ice/water, acidified with hydrochloric acid (15 mL, 1 N) and partitioned between water and ethyl acetate. The organic portion was washed with brine, combined, dried over Na2SO4, filtered and concentrated. The crude product precipitated as brown solid from the concentrated solution and was used without further purification in the next step. MS (ESI, m/z): 268.1 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-2d70d6f69d29454781b85846bff6c1c6
Source noteuspto-grants-2016_08