HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-Bromo-3,6,8-tri(4-methylphenyl)pyrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,3,6-Tri(4-methylphenyl)pyrene | HCID 86628591 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromo-3,6,8-tri(4-methylphenyl)pyrene | HCID 86628592 | 85.7% |
Reaction Steps
Next, a mixed solution of 1.5 g of 1,3,6-tri(4-methylphenyl)pyrene, 0.68 g of N-bromosuccinimide and 30 ml of dimethylformamide was stirred under a nitrogen gas flow at 60° C. for 6 hours. After cooling to room temperature, 50 ml of water was injected, followed by extraction with 100 ml of dichloromethane. The organic layer was washed twice with 50 ml of water, dried over magnesium sulfate and then evaporated. The resultant concentrate was purified by silica gel column chromatography and then vacuum-dried to obtain 1.5 g of 1-bromo-3,6,8-tri(4-methylphenyl)pyrene as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729530B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-b353cb3c5dad469cb475ed4782b41790 |
| Source note | uspto-grants-2014_05 |