HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914400Generated: November 2, 2026
Dimethylformamide → 1-(3,5-Dichlorophenyl)-6-(4-methylphenyl)pyrene
https://huagongshe.com/reaction/1914400
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3,5-Dichlorophenylboronic acid | HCID 2734331 | — |
| Reactant | 1-Bromo-6-(4-methylphenyl)pyrene | HCID 86101361 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(3,5-Dichlorophenyl)-6-(4-methylphenyl)pyrene | HCID 86101381 | 58.4% |
Reaction Steps
A mixed solution of 8.0 g of 1-bromo-6-(4-methylphenyl)pyrene, 4.5 g of 3,5-dichlorophenylboronic acid, 9.2 g of tripotassium phosphate, 1.4 g of tetrabutylammonium bromide, 97 mg of palladium acetate and 215 ml of dimethylformamide was heated and stirred under a nitrogen gas stream at 120° C. for 5 hours. The solution was cooled to room temperature and 1.0 L of water was poured into the solution, followed by extraction with 600 ml of dichloromethane. The organic layer was washed twice with 200 ml of water, dried over magnesium sulfate and then filtered through Celite. The filtrate was evaporated and the residue was washed twice with 200 ml of ethyl acetate, and then the precipitated solid was collected by filtration. The precipitated solid was recrystallized from 100 ml of dimethylformamide and then vacuum-dried to obtain 5.5 g of 1-(3,5-dichlorophenyl)-6-(4-methylphenyl)pyrene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08610345B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-52661c09f5294f2fb52ef56def469bcd |
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| Source note | uspto-grants-2013_12 |
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