HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 9-Acetyl-3-bromocarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Bromocarbazole | HCID 252446 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 9-Acetyl-3-bromocarbazole | HCID 1714879 | 52.1% |
Reaction Steps
A solution of 3-bromo-9H-carbazole (10.00 g, 40.6 mmol), acetic anhydride (8.30 g, 81 mmol) together with 2 drops of H2SO4 in chloroform (150 mL) was refluxed overnight. After cooling to room temperature, the solution was washed with water. Upon evaporation of the solvent, the crude product was purified by crystallization from hexane/DCM and hexane/EtOAc to yield 1-(3-bromo-9H-carbazol-9-yl)ethanone (6.1 g, 51% yield) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748012B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-448e779b27c0471baaa8051f1674588c |
| Source note | uspto-grants-2014_06 |