HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656849Generated: October 26, 2026
N-bromobutanimide → Bromo-tert-butylpyrene
https://huagongshe.com/reaction/656849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Pyrene, 1-(1,1-dimethylethyl)- | HCID 187956 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Bromo-tert-butylpyrene | HCID 86639773 | 90% |
Reaction Steps
Next, 25.0 g (0.10 mol) of tert-butylpyrene and 250 ml of DME (1,2-dimethoxyethane) were charged in a reaction vessel, and the mixture was cooled to 0° C. Next, NBS was added in an amount of 4 equivalents relative to tert-butylpyrene, and the resulting mixture was stirred overnight at room temperature, filtered, and recrystallized to produce 29.5 g of bromo-tert-butylpyrene crystals in a yield of 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071993B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-5f32d15fadfa4e929daf62d905b40864 |
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| Source note | uspto-grants-2011_12 |
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