HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404887Generated: October 31, 2026
N-bromobutanimide → 1-Bromo-7-(tert-butyl)pyrene
https://huagongshe.com/reaction/1404887
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Tert-butylpyrene | HCID 11817768 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-7-(tert-butyl)pyrene | HCID 49765730 | 81% |
Reaction Steps
To a mixed solution of 120 g (content 79.2%) of 2-t-butylpyrene, and 3000 ml of tetrahydrofuran was added 69.66 g of N-bromosuccinimide under a nitrogen stream. This mixed solution was stirred at 30° C. for about 3 hours, and concentrated, 500 ml of methanol was added, and the mixture was stirred for about 1 hour, and filtered. To the resulting solid was added 500 ml of hexane, and the mixture was heated and stirred for about 1 hour, and filtered. After the resultant was vacuum dried, 106.9 g of 1-bromo-7-t-butylpyrene was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08916275B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-daba8cb79ec94af9a151687ca18165e3 |
|---|
| Source note | uspto-grants-2014_12 |
|---|