HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587727Generated: October 28, 2026
Phthalic Anhydride → 2-(4-bromoanilino)-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/587727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-(4-bromoanilino)-1H-isoindole-1,3(2H)-dione | HCID 16044339 | 84% |
Reaction Steps
To a stirred solution of (4-bromophenyl)hydrazine hydrochloride (0.5 g, 2.2 mmol) in AcOH (8 mL) was added phthalic anhydride (0.398 g, 2.690 mmol), and the reaction mixture was stirred at 130° C. for 1 h under a nitrogen atmosphere. The reaction mixture was quenched with satd aqueous NaHCO3 solution and filtered to give a solid. Purification by column chromatography (SiO2, O-10% EtOAc in petroleum ether) afforded the title compound as a solid (60 mg, 84%): mp 205-206° C.; 1H NMR (400 MHz, CDCl3) δ 8.71 (s, 1H), 7.99 (m, 4H), 7.32 (d, J=8.8 Hz, 2H), 6.79 (d, J=8.8 Hz, 2H); ESIMS m/z 314.95 ([M−H]−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09226501B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-7fd5e8ffb80d46baa608bec8ddc9e2e3 |
|---|
| Source note | uspto-grants-2016_01 |
|---|