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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656849Generated: October 26, 2026

N-bromobutanimide → Bromo-tert-butylpyrene

https://huagongshe.com/reaction/656849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantPyrene, 1-(1,1-dimethylethyl)-HCID 187956—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductBromo-tert-butylpyreneHCID 8663977390%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071993B2
Source datasetuspto-grants-2011_12
ORD IDord-5f32d15fadfa4e929daf62d905b40864
Source noteuspto-grants-2011_12