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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937527Generated: November 1, 2026

3-Aminophenylboronic acid → HCID 21925704, compound

https://huagongshe.com/reaction/1937527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminophenylboronic acidHCID 92269—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 21925704HCID 21925704183.8%

Reaction Steps

3-Aminophenylboronic acid (3.9 g), 5 g 5-bromo-2-fluoronitrobenzene, 0.8 g tetrakis(triphenylphosphine)palladium and 23 mL of 2 M sodium bicarbonate solution in 50 mL of toluene were refluxed under nitrogen for 2.5 hours. The reaction mixture was poured into 200 mL of ice water and the mixture extracted three times with 50 mL of ethyl acetate. The combined organic layers were washed with 50 mL of water and 20 mL of brine, dried over anhydrous sodium sulfate and concentrated to give 9.7 g (92% yield) of 2-fluoro-5-(3-aminophenyl)nitrobenzene as a dark brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395734B1
Source datasetuspto-grants-2002_05
ORD IDord-7949be8bba6e48a787536348c6887fac
Source noteuspto-grants-2002_05