HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 9-([1,1'-Biphenyl]-4-yl)-3-iodo-9H-carbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 9-(4-Biphenylyl)carbazole | HCID 412897 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 9-([1,1'-Biphenyl]-4-yl)-3-iodo-9H-carbazole | HCID 59132906 | 98.8% |
Reaction Steps
3.2 g (10 mmol) of 9-(4-biphenylyl)carbazole was dissolved in a mixed solution of 200 mL of glacial acetic acid, 200 mL of toluene, and 50 mL of ethyl acetate. 2.3 g (10 mmol) of N-iodosuccinimide was slowly added thereto. The mixture was stirred overnight (for about 24 hours) and then washed with water, a sodium thiosulfate water solution, and a saturated sodium chloride solution. Magnesium sulfate was added thereto to remove water and filtered to obtain a filtrate. The filtrate was concentrated, mixed with acetone and hexane, and then recrystallized with ultrasonic wave. This was filtered to obtain a residue. The residue was collected and dried. 4.4 g (yield: 98%) of 3-iodo-9-(4-biphenylyl)carbazole, which was beige powder, was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07649197B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-b31f760a84424345876e9bcb69486b85 |
| Source note | uspto-grants-2010_01 |