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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404890Generated: November 1, 2026

N-bromobutanimide → HCID 86660757, compound

https://huagongshe.com/reaction/1404890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 86660758HCID 86660758—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86660757HCID 8666075785.3%

Reaction Conditions

Temperature30 °C

Reaction Steps

Then, to a mixed solution of 8.65 g of 1-(4-biphenylyl)-7-t-butylpyrene, and 126 ml of tetrahydrofuran was added 4.1 g of N-bromosuccinimide under a nitrogen stream. This mixed solution was stirred at 30° C. for about 3 hours, and concentrated, 126 ml of methanol was added, and the mixture was stirred for about 1 hour, and filtered. To the resulting solid was added 30 ml of tetrahydrofuran, the mixture was heated and dissolved, 180 ml of methanol was added, and the mixture was stirred for about 1 hour, and filtered. After the resultant was purified by silica gel column chromatography, the solid obtained by evaporation was washed with 126 ml of methanol, and vacuum dried to obtain 8.8 g of 1-bromo-3-(4-biphenylyl)-7-t-butylpyrene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916275B2
Source datasetuspto-grants-2014_12
ORD IDord-a21b9ca106ab4d85b3de5d0178c27a3a
Source noteuspto-grants-2014_12