HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 3-Bromo-9-phenylcarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 9-Phenylcarbazole | HCID 70851 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Bromo-9-phenylcarbazole | HCID 18942624 | 99% |
Reaction Steps
In a 1000 mL Erlenmeyer flask, 24 g (100 mmol) of 9-phenyl-9H-carbazole, 18 g (100 mmol) of N-bromosuccinimide, 450 mL of toluene, and 200 mL of ethylacetate were added, and the mixture was stirred at room temperature for 45 hours. After the reaction, the resulting mixture was washed with water, and the organic layer is dried with magnesium sulfate. The mixture was filtered, and the resulting filtrate was concentrated to give 32 g of the desired substance 3-bromo-9-phenyl-9H-carbazole in 99% yield. The synthetic scheme of 3-bromo-9-phenyl-9H-carbazole is shown in the scheme (C-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08283055B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-579d7af1db214a7f8b43e31cc1234caa |
| Source note | uspto-grants-2012_10 |