Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodo-4-(trifluoromethoxy)benzene | HCID 2777294 | — |
| Reactant | HCID 10286124 | HCID 10286124 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86593496 | HCID 86593496 | 44.4% |
Reaction Steps
A mixture of 0.6 g (2.6 mmol) 5-(4-trifluoromethoxy-phenyl)-1H-indole, 0.53 mL (2.8 mmol) 4-(trifluoromethoxy)iodobenzene, 0.075 g (0.52 mmol) copper(I) bromide and 0.54 g (3.9 mmol) K2CO3 in 10 mL anhydrous N-methylpyrrolidinone was heated to reflux overnight with stirring. The reaction was allowed to cool and was then poured into 200 mL of water. The aqueous solution was shaken with 200 mL ethyl acetate, the combined aqueous and organic phases were filtered, and the organic phase was separated. The aqueous phase was extracted once more with 200 mL ethyl acetate and the combined organic phases were washed with brine and concentrated. The crude product was chromatographed on silica (5–7% EtOAc-hexane as elutant) to afford 0.505 g (44% yield) of 1,5-bis-(4-trifluoromethoxy-phenyl)-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259182B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-afc8605e788c46b58832c41f8e01e78d |
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| Source note | uspto-grants-2007_08 |
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