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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Reactant | 3-Amino-4-iodo-6-bromophthalimide | HCID 68488717 | — |
| Catalyst | Cuprous 2-thiophenecarboxylate | HCID 11194830 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Amino-4,6-diphenylphthalimide | HCID 68491185 | 11% |
| Product | 3-Amino-4-phenyl-6-bromophthalimide | HCID 68491804 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745641B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-a7a633f7302e4533ab7835672ef5448a |
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| Source note | uspto-grants-2010_06 |
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