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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-t-Butyl-1-(4-chlorophenyl)pyreneHCID 86660755—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-7-t-butyl-3-(4-chlorophenyl)pyreneHCID 8666075691.7%

Reaction Conditions

Temperature30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916275B2
Source datasetuspto-grants-2014_12
ORD IDord-9d971f30491243c4b343586e2946127c
Source noteuspto-grants-2014_12