HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-[2-nitro-5-(2-cyano-4-trifluoromethylphenoxy)benzoyl]phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | 5-[2-Cyano-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl chloride | HCID 20229922 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-nitro-5-(2-cyano-4-trifluoromethylphenoxy)benzoyl]phthalimide | HCID 20472961 | — |
Reaction Steps
The N-potassium salt of phthalimide (0.025 mole) dissolved in dimethylformamide (50 ml) and 2-nitro-5-(2-cyano-4-trifluoromethylphenoxy)benzoyl chloride (0.025 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at room temperature for a period of about 8 hours. After this time the mixture is poured into water (150 ml) and is extracted twice with toluene. The toluene extracts are combined and stripped of solvent leaving a solid residue. This residue is recrystallized to yield the desired product N-[2-nitro-5-(2-cyano-4-trifluoromethylphenoxy)benzoyl]phthalimide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04427441 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-8f120d4b099b4c78ad14565be1306175 |
| Source note | uspto-grants-1984_01 |