Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | HCID 68812137 | HCID 68812137 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68812092 | HCID 68812092 | — |
Reaction Steps
A slurry prepared from 34.3 g (0.115 mole) of N,N′-diacetyl-2,6-diaminodibenzodioxin, 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 slurry was cooled to room temperature, 500 ml of methylene chloride and 500 ml of water were added, and a precipitate was filtered off. 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. The product was used without purification in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605277B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-3a0848a8324c447a98293dbd204d12c9 |
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| Source note | uspto-grants-2009_10 |
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