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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004720Generated: October 31, 2026

3-Aminophenylboronic acid → HCID 21925704, compound

https://huagongshe.com/reaction/1004720

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 numberUS06051593
Source datasetuspto-grants-2000_04
ORD IDord-190ae387ae494380b9e1eacbb3b24c41
Source noteuspto-grants-2000_04