HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-4,6-diphenyl-1,3,5-triazine → 5-(4,6-Diphenyl-1,3,5-triazin-2-yl)-7,7-dimethyl-5,7-dihydroindeno[2,1-b]carbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-4,6-diphenyl-1,3,5-triazine | HCID 19698 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7,7-Dimethyl-5,7-dihydroindeno[2,1-b]carbazole | HCID 66585204 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4,6-Diphenyl-1,3,5-triazin-2-yl)-7,7-dimethyl-5,7-dihydroindeno[2,1-b]carbazole | HCID 66585242 | — |
Reaction Steps
8 g (28.2 mmol) of 12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene are dissolved in 225 ml of dimethylformamide under a protective-gas atmosphere, and 1.5 g of NaH, 60% in mineral oil (37.5 mmol), are added. After 1 h at room temperature, a solution of 2-chloro-4,6-diphenyl-1,3,5-triazine (8.5 g, 31.75 mmol) in 75 ml of dimethylformamide is added dropwise. The reaction mixture is then stirred at room temperature for 12 h. After this time, the reaction mixture is poured onto ice and extracted three times with dichloromethane. The combined organic phases are dried over Na2SO4 and evaporated. The residue is extracted with hot toluene. The yield is 12 g (23 mmol, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126970B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-e6406c0fa0f94573bfc04b816a201e57 |
| Source note | uspto-grants-2015_09 |