HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 9-Acetyl-3-bromocarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Bromocarbazole | HCID 252446 | — |
| Product | 9-Acetyl-3-bromocarbazole | HCID 1714879 | — |
Reaction Steps
20 g of 3-bromocarbazole was converted to its acetyl derivative by refluxing with acetic anhydride (3 vol) with traces of conc. sulfuric acid. Aqueous workup yielded an off-white solid, which was then washed with n-hexane and dried under vacuum to obtain 23 g 9-acetyl-3-bromocarbazole, quantitatively. And N-acetyl derivative of carbazole, benzocarbaole and dibenzocarbazoles were prepared following the same procedure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353085B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-47ec478568da421fbd7d36378cc19fdc |
| Source note | uspto-grants-2016_05 |