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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404352Generated: October 28, 2026

Dimethylformamide → Methyl 2'-fluoro-5'-(methyloxy)-2-nitro-1,1'-biphenyl-4-carboxylate

https://huagongshe.com/reaction/404352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-chloro-3-nitrobenzoateHCID 735797—
Reactant2-Fluoro-5-methoxyphenylboronic acidHCID 4157211—
CatalystHCID 178418397HCID 178418397—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 2'-fluoro-5'-(methyloxy)-2-nitro-1,1'-biphenyl-4-carboxylateHCID 5770633599.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of methyl 4-chloro-3-nitrobenzoate T20.1 (10.00 g, 46 mmol) (commercially available from Sigma-Aldrich, St. Louis, Mo., USA) in DMF (15.00 mL, 194 mmol) at 23° C. was added 2-fluoro-5-methoxyphenylboronic acid (12 g, 70 mmol) (commercially available from Sigma-Aldrich, St. Louis, Mo., USA), and potassium carbonate (19 g, 139 mmol). Tetrakis(triphenylphosphine)palladium (2.1 g, 1.9 mmol) was then added to the mixture, and the mixture was heated at 90° C. for 18 hours. The mixture was then cooled to room temperature, diluted with brine and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was purified on silica gel (0-40% EtOAc in hexanes) to yield T20.2 as a colorless oil (14.00 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748462B2
Source datasetuspto-grants-2014_06
ORD IDord-c72ebf4d9431432ba8136ca67ae5d721
Source noteuspto-grants-2014_06