HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophthalimide → HCID 41956059, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophthalimide | HCID 6969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 41956059 | HCID 41956059 | 78% |
Reaction Steps
A solution of 5-nitroisoindoline-1,3-dione (1.00 g, 5.20 mmol), benzyl 2-bromoacetate (1.225 ml, 7.81 mmol) and K2CO3 (1.079 g, 7.81 mmol) in DMF (10 ml) was heated at 90° C. for 2 hours. The insoluble inorganic salts were filtered off, and the filtrate was diluted with ethyl acetate and washed with 1N HCl and with brine. The organic layer was dried over Na2SO4 and the solvent was removed under vacuum. The residue was purified by crystallization from MeOH to afford benzyl 2-(5-nitro-1,3-dioxoisoindolin-2-yl)acetate (1.39 g, 4.08 mmol, 78% yield, MS/ESI+ not detectable [MH]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024027B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-f1e2b2f59ca148f1b1bb7cceee355b19 |
| Source note | uspto-grants-2015_05 |