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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627764Generated: October 25, 2026

Ethanol → Methyl 5'-fluoro-2'-nitrobiphenyl-2-carboxylate

https://huagongshe.com/reaction/627764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-4-fluoro-1-nitrobenzeneHCID 2756993—
Reactant2-(Methoxycarbonyl)benzeneboronic acidHCID 2773496—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventDichloromethaneHCID 6344—
ProductMethyl 5'-fluoro-2'-nitrobiphenyl-2-carboxylateHCID 6729693656.9%

Reaction Steps

To a microwave vessel was added 2-(methoxycarbonyl)phenylboronic acid (63.4 mg, 0.352 mmol), 2-bromo-4-fluoro-1-nitrobenzene (77 mg, 0.35 mmol), diacetoxypalladium (0.93 mg, 4.1 μmol) and dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (3.47 mg, 8.45 μmol). Ethanol (1760 μl) and sodium carbonate (176 μl, 0.352 mmol) were added and the mixture was reacted in a microwave reactor at 100° C. for 30 min. The reaction mixture was diluted with dichloromethane, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by preparative thin layer chromatography (eluant: 9:1 hexane/ethyl acetate) to provide methyl 5′-fluoro-2′-nitrobiphenyl-2-carboxylate (37a, 54.8 mg, 0.199 mmol, 56.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309279B2
Source datasetuspto-grants-2016_04
ORD IDord-de5216e5a08342268e6cdce9a3e4ecd9
Source noteuspto-grants-2016_04