HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dimethylaniline → 1,3(2H,4H)-Isoquinolinedione, 2-(2,6-dimethylphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dimethylaniline | HCID 6896 | — |
| Reactant | Homophthalic anhydride | HCID 12801 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,3(2H,4H)-Isoquinolinedione, 2-(2,6-dimethylphenyl)- | HCID 182751 | 68% |
Reaction Steps
0.67 g (4.13 mmol) of homophthalic anhydride and 0.4 g (3.30 mmol) of 2,6-dimethylaniline were mixed, and melted at a temperature of 200° C. for 1 hour. The reactant was dissolved in ethyl acetate, washed with aqueous NaHCO3 solution, with water and then with saturated aqueous sodium chloride, dried over anhydrous MgSO4, and subjected to filtration with a folded filter paper. The filtrate was concentrated and evaporated to dryness. The residue was recrystallized by using a mixture of CH2Cl2 and hexane, to obtain 0.565 g (yield 68%) of the specified substance as light yellow granulated crystals. It showed the following physical properties and analyzed values.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06429212B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-552f155c24d8450bbf5f748cf90a8017 |
| Source note | uspto-grants-2002_08 |