HuagongsheHuagongshe Chemistry Print Report · For research reference only
Urea → 2-(3-bromo-2-oxopropyl)-2,3-dihydro-1H-isoindole-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Phthalimidoacetone | HCID 235046 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-bromo-2-oxopropyl)-2,3-dihydro-1H-isoindole-1,3-dione | HCID 222037 | 3% |
Reaction Steps
To a solution of phthalimidoacetone (4.04 g, 19.9 mmol) in methanol (100 mL) was added urea (1.19 g, 19.9 mmol) and bromine (3.18 g, 19.9 mmol) and the resulting solution was stirred at room temperature overnight. The reaction was concentrated in vacuo and the residue taken up in DCM (150 mL) and water (50 mL). The layers were separated and the organic layer was dried, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (EA/hexanes=0/100→50/50) to give 159 mg (3% yield) of the title compound. 1H NMR (300 MHz, CDCl3) δ: 7.90-7.86 (m, 2H), 7.79-7.73 (m, 2H), 4.78 (s, 2H), 4.01 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796268B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-0d8c31b116df402cbece456bb5ac35e4 |
| Source note | uspto-grants-2014_08 |