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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452172Generated: October 25, 2026

Water → 4-Amino-3-methyl-5-nitrobiphenyl

https://huagongshe.com/reaction/452172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Bromo-2-methyl-6-nitroanilineHCID 522679—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product4-Amino-3-methyl-5-nitrobiphenylHCID 6721050881.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

[step 2] Under a nitrogen atmosphere, 4-bromo-6-methyl-2-nitroaniline (2.80 g, 12.1 mmol) obtained in step 1 was dissolved in DMF (60 mL), phenylboronic acid (4.40 g, 36.3 mmol), cesium carbonate (7.90 g, 24.2 mmol) and tetrakis(triphenylphosphine)palladium (1.40 g, 2.42 mmol) were added, and the mixture was stirred at 100° C. for 4 hr. Water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1 to 0/1) to give 4-amino-3-methyl-5-nitrobiphenyl (2.25 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486980B2
Source datasetuspto-grants-2013_07
ORD IDord-4f61106da3c847a48a7a558520e1035e
Source noteuspto-grants-2013_07