HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5,6-Tetrabromophthalimide → N-(pentachlorobenzoyl)-3,4,5,6-tetrabromophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5,6-Tetrabromophthalimide | HCID 90490 | — |
| Reactant | Pentachlorobenzoyl chloride | HCID 1812012 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(pentachlorobenzoyl)-3,4,5,6-tetrabromophthalimide | HCID 21546571 | — |
Reaction Steps
The potassium salt of 3,4,5,6-tetrabromophthalimide (0.10 mole) and dioxane (1200 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. Pentachlorobenzoyl chloride (0.10 mole) is then added dropwise, with stirring, to the reaction mixture at room temperature. After the addition is completed the reaction mixture is heated at reflux for a period of about 1 hour. After this time the reaction mixture is filtered and the filtrate is stripped of solvent to yield the desired product N-(pentachlorobenzoyl)-3,4,5,6-tetrabromophthalimide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03950307 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-4fa767ea5a5e4bfbb9da94eb823fd3b1 |
| Source note | uspto-grants-1976_04 |