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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760140Generated: October 30, 2026

N-bromobutanimide → 3-bromo-2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-one

https://huagongshe.com/reaction/1760140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-oneHCID 22597178—
SolventDimethylformamideHCID 6228—
Product3-bromo-2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-oneHCID 2259716777.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A 500 ml three neck round bottom flask was equipped with a mechanical stirrer, heating mantle and condenser. To the flask was added 28.5 g 2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-one, 15 g N-bromosuccinimide and 160 g DMF. The mixture was agitated well, heated to 50° C. and held at 50° C. for two hours. The mixture was cooled to 0° C. and, after several hours, the mixture was filtered to recover the solid product. The solid was suspended in 250 g water, stirred well and filtered. The yellow solid product was dried in a 50° C. oven for ten hours to give 27.1 g of 3-bromo-2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-one with melting point of 85-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06841236B2
Source datasetuspto-grants-2005_01
ORD IDord-71947c9067954a6680e034bb3f27267a
Source noteuspto-grants-2005_01