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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966494Generated: October 25, 2026

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

https://huagongshe.com/reaction/1966494

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 mmol) 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 numberUS08420596B2
Source datasetuspto-grants-2013_04
ORD IDord-7cc4ca40e53e4282bbf71bf8066e04f1
Source noteuspto-grants-2013_04