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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880973Generated: October 30, 2026

Ethyl Acetate → 2-Fluoro-3-methoxy-4-nitrobenzonitrile

https://huagongshe.com/reaction/1880973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactant1-Bromo-2-fluoro-3-methoxy-4-nitrobenzeneHCID 57955589—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystPalladiumHCID 23938—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylacetamideHCID 31374—
Product2-Fluoro-3-methoxy-4-nitrobenzonitrileHCID 57955549433.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 1-Bromo-2-fluoro-3-methoxy-4-nitrobenzene (250 mg, 1 mmol) and zinc cyanide (70 mg, 0.6 mmol) were stirred in DMA (5 mL) and purged with nitrogen. The palladium catalyst, Pd2(dba)3 (92 mg, 0.1 mmol), and the ligand, Davephos (79 mg, 0.2 mmol), were added and the reaction mixture was stirred at 90° C. overnight. It was then cooled to rt., diluted to ethyl acetate, washed with brine. Organic dried, concentrated and purified by flash column (EtOAc/Hexane=1:20) to give 170 mg product (87%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 4.15 (s, 3 H) 7.42 (dd, J=9.0, 6.2 Hz, 1 H) 7.65 (dd, J=9.0, 1.9 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318727B2
Source datasetuspto-grants-2012_11
ORD IDord-24f3f53966134e4e8605a733e9c720c5
Source noteuspto-grants-2012_11