HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(2,4,6-tribromobenzoyl)-3,4-dibromohexahydrophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,4,6-tribromobenzoyl Chloride | HCID 11234266 | — |
| Reactant | 3,4-Dibromohexahydrophthalimide | HCID 21542796 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(2,4,6-tribromobenzoyl)-3,4-dibromohexahydrophthalimide | HCID 21542800 | — |
Reaction Steps
3,4-Dibromohexahydrophthalimide (0.10 mole), benzene (300 ml) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2,4,6-Tribromobenzoyl chloride (0.10 mole) is then added dropwise to the flask with stirring at room temperature. After the addition is completed the reaction mixture is heated at reflux with continued stirring for a period of about 1 hour. After this time the reaction mixture is filtered and the filtrate is washed with water. The washed filtrate is then dried over anhydrous magnesium sulfate, filtered ans stripped of solvent under reduced pressure to yield the desired product N-(2,4,6-tribromobenzoyl)-3,4-dibromohexahydrophthalimide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03953397 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-f33b8bfbee8b4bce8cc143e67b2fe5ac |
| Source note | uspto-grants-1976_04 |