HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404889Generated: October 31, 2026
N-bromobutanimide → 1-Bromo-7-t-butyl-3-(4-chlorophenyl)pyrene
https://huagongshe.com/reaction/1404889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-t-Butyl-1-(4-chlorophenyl)pyrene | HCID 86660755 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-7-t-butyl-3-(4-chlorophenyl)pyrene | HCID 86660756 | 91.7% |
Reaction Steps
Then, to a mixed solution of 100.6 g of 7-t-butyl-1-(4-chlorophenyl)pyrene, and 1638 ml of tetrahydrofuran was added 53.5 g of N-bromosuccinimide under a nitrogen stream. This mixed solution was stirred at 30° C. for about 5 hours, and concentrated, 984 ml of methanol was added, and the mixture was stirred for about 1 hour, and filtered. To the resulting solid was added 539 ml of hexane, and the mixture was heated and stirred for about 1 hour, and filtered. After the resultant was vacuum dried, 112.0 g of 1-bromo-7-t-butyl-3-(4-chlorophenyl)pyrene was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08916275B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-9d971f30491243c4b343586e2946127c |
|---|
| Source note | uspto-grants-2014_12 |
|---|