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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-one | HCID 22597178 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-bromo-2-[(2-ethylhexyl)oxy]-7H-benzo[de]anthracene-7-one | HCID 22597167 | 77.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06841236B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-71947c9067954a6680e034bb3f27267a |
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| Source note | uspto-grants-2005_01 |
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