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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20997Generated: October 27, 2026

Ammonium Chloride → 3-Amino-4-phenyl-6-bromophthalimide

https://huagongshe.com/reaction/20997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPhenylboronic AcidHCID 66827—
ReactantChloroform methanolHCID 21584188—
Reactant3-Amino-4-iodo-6-bromophthalimideHCID 68488717—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-4,6-diphenylphthalimideHCID 6849118511%
Product3-Amino-4-phenyl-6-bromophthalimideHCID 6849180466%

Reaction Steps

3-Amino-4-iodo-6-bromophthalimide (80.0 mg, 0.218 mmol) was dissolved in THF (5.6 mL), and the solution was added with phenylboronic acid (80 mg, 0.65 mmol), tetrakis(triphenylphosphine)palladium (20 mg, 0.017 mmol) and copper(I) thiophene-2-carboxylate (125 mg, 0.65 mmol), followed by stirring at room temperature for 14 hours under argon atmosphere. The reaction mixture was added with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by slurry using isopropylether, then by preparative thin-layer chromatography (chloroform/methanol=60/1) to obtain 3-amino-4-phenyl-6-bromophthalimide (46 mg, yield 66%) and 3-amino-4,6-diphenylphthalimide (7.6 mg, yield 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-a7a633f7302e4533ab7835672ef5448a
Source noteuspto-grants-2010_06