HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dichlorobenzoyl chloride → N-(2,5-dichlorobenzoyl)-3,4,5,6-tetrabromophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dichlorobenzoyl chloride | HCID 17945 | — |
| Reactant | 3,4,5,6-Tetrabromophthalimide | HCID 90490 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(2,5-dichlorobenzoyl)-3,4,5,6-tetrabromophthalimide | HCID 21546568 | — |
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. 2,5-Dichlorobenzoyl 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-(2,5-dichlorobenzoyl)-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-3681e675bfe74b40b17b30aa4395d7ba |
| Source note | uspto-grants-1976_04 |