HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromosuccinimide → 10-(Biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromosuccinimide | HCID 38309 | — |
| Reactant | 10-(Biphenyl-4-yl)-2-phenyl-9,10-dihydroacridine | HCID 67523530 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 10-(Biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine | HCID 67523480 | 70% |
Reaction Steps
10-(biphenyl-4-yl)-2-phenyl-9,10-dihydroacridine (7.8 g, 19.0 mmol) was added with chloroform (300 ml), and with bromosuccinimide (3.7 g, 21.0 mmol). The resultant solution was stirred at room temperature for 2 hours. After the reaction was completed, the resultant solution was washed with distilled water. Then, an organic layer was extracted and dried with sodium sulfate so as to remove the solvent. The residue was purified by silica gel column chromatography (methylene chloride/n-hexane (1/10)) to obtain 10-(biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine compound (pale yellow solid, 6.5 g, yield 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08597802B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-a96a6ae6207e48c5a850b724648051a9 |
| Source note | uspto-grants-2013_12 |