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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528388Generated: November 3, 2026

Hydrochloric Acid → 5-(3-Chloro-4-fluorophenyl)-6-(2,2,2-trifluoroethoxy)nicotinic acid

https://huagongshe.com/reaction/1528388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 2734660—
Reactant5-Bromo-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxylic acidHCID 58192592—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product5-(3-Chloro-4-fluorophenyl)-6-(2,2,2-trifluoroethoxy)nicotinic acidHCID 6667884263%

Reaction Conditions

Temperature90 °C

Reaction Steps

5-Bromo-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxylic acid (CAN 1211586-75-2; 1.5 g; 5.0 mmol) was dissolved in toluene (35 mL) an DMF (2 mL). To this solution was added 1,1′-bis(diphenylphosphino)-ferrocene-palladium(II)dichloride dichloromethane complex (204 mg, 250 μmol), followed by 3-chloro-4-fluorophenylboronic acid (CAN 144432-85-9; 959 mg, 5.5 mmol) and 2M-Na2CO3 (20.0 mL 40.0 mmol). The reaction mixture was heated to 90° C. and stirred for 4 h, cooled and poured into 100 mL ice water, acidified with 45 mL 2N—HCl and extracted ethyl acetate. The organic layers were combined, dried with Na2SO4 and concentrated in vacuo. The crude material was crystallized from heptane:ethyl acetate (5:1) to yield 1.1 g (63%) of the title compound as light grey solid; LC-MS (UV peak area/ESI): 97%, 348.0066 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090599B2
Source datasetuspto-grants-2015_07
ORD IDord-fd8d00830a164aec958162d0367b85c1
Source noteuspto-grants-2015_07