HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-Bromo-3,6,8-tri(4-methylnaphthalene-1-yl)pyrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,3,6-Tri(4-methylnaphthalene-1-yl)pyrene | HCID 86628594 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromo-3,6,8-tri(4-methylnaphthalene-1-yl)pyrene | HCID 86628593 | 70.1% |
Reaction Steps
A mixed solution of 1.9 g of the above-mentioned 1,3,6-tri(4-methylnaphthalene-1-yl)pyrene, 0.64 g of N-bromosuccinimide and 15 ml of dimethylformamide was stirred under nitrogen gas stream at a temperature of 60° C. for 6 hours. After cooling the mixed solution to room temperature, 50 ml of water was injected thereinto to extract therefrom with 100 ml of dichloromethane. The organic layer was washed twice with 50 ml of water, dried by magnesium sulfate and thereafter concentrated by evaporation. The organic layer was purified by silica gel column chromatography and thereafter vacuum dried under a temperature of 70° C. to obtain 1.5 g of 1-bromo-3,6,8-tri(4-methylnaphthalene-1-yl)pyrene as pale-yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07901794B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-ad961cfacc5549c48c88364599b9bdce |
| Source note | uspto-grants-2011_03 |