HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905536Generated: October 30, 2026
Quinoline → 2,7-bis(N-phenylacetylamino)dibenzodioxin
https://huagongshe.com/reaction/905536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | 2,7-Bis(acetylamino)dibenzodioxin | HCID 57892507 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,7-bis(N-phenylacetylamino)dibenzodioxin | HCID 67389094 | — |
Reaction Steps
A slurry prepared from 34.3 g (0.115 mole) of 2,7-bis(acetylamino)dibenzodioxin, 96.4 g (0.576 mole) of iodobenzene, 48.2 g (0.253 mole) of copper (I) iodide, 63.6 g (0.460 mole) of potassium carbonate, and 1500 ml of quinoline was heated with stirring at 170° C. for 48 hours. The reaction mixture was cooled to room temperature, 500 ml of methylene chloride and 500 ml of water were added, and a precipitate was separated by filtration. To the filtrate was added 500 ml of water and the organic layer was separated from the aqueous layer. The organic layer was concentrated and dried under reduced pressure to give 79.4 g of a crude product which was used without purification in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012606B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-9374108a7280443e8dba6ab2123f1ac4 |
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| Source note | uspto-grants-2011_09 |
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