HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-{2-[2-(2-Methoxyethoxy)ethoxy]ethyl}-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Methoxyethoxyethoxy-1-iodoethane | HCID 23352112 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-{2-[2-(2-Methoxyethoxy)ethoxy]ethyl}-1H-isoindole-1,3(2H)-dione | HCID 57206461 | — |
Reaction Steps
1.3 g of potassium phthalimide, 2-methoxyethoxyethoxy-1-iodoethane and 5 ml of dimethylformamide were fed into a 100 ml short-neck flask provided with a reflux condenser. The resultant mixture was heated at 90° c. for 3 hours. 100 ml of ethyl acetate was added thereto and the resultant mixture was cooled to room temperature. White precipitates thus obtained were suction-filtered, and the filtrate was washed with 100 ml of water. The obtained ethyl acetate layer was dried over magnesium sulfate, and ethyl acetate was distilled off under reduced pressure to obtain the intended compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05599825 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-b6cfd3f61fe945c0a3fde048ea7bb1b4 |
| Source note | uspto-grants-1997_02 |