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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744360Generated: October 30, 2026

Toluene → 4-Fluoro-3'-methoxy-3-nitrobiphenyl

https://huagongshe.com/reaction/1744360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant(3-Methoxyphenyl)boronic acidHCID 2734370—
Reactant4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product4-Fluoro-3'-methoxy-3-nitrobiphenylHCID 10490702—

Reaction Steps

4-Bromo-1-fluoro-2-nitro-benzene (5 gms.), 3.85 gms. 3-methoxyphenylboronic acid and 22 mL of a 2M aqueous solution of sodium carbonate are suspended in 100 mL of a 1:1 (v:v) mix of toluene and ethanol. The resulting suspension is then treated with 0.8 gms. tetrakis(triphenylphosphine)palladium (0) at room temperature. The reaction mixture is then heated at reflux for 12 h. The reaction mixture is subsequently concentrated in vacuo, and the resulting residue is taken up in ethyl acetate (200 mL). The ethyl acetate solution is then washed successively with water (2×200 mL), and brine (2×200 mL). The organic layer is then dried by filtering through phase separator paper and concentrated in vacuo to yield 7.19 gms. of crude product. The crude product is then recrystallized from hot ethanol yielding 4-fluoro-3′-methoxy-3-nitro-biphenyl as a yellow-white solid in the amount of 4.767 gms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015220B2
Source datasetuspto-grants-2006_03
ORD IDord-1b8b52b8bfe2444eb1e9806e4b884bf4
Source noteuspto-grants-2006_03