Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | HCID 22416884 | HCID 22416884 | — |
| Reactant | HCID 22416911 | HCID 22416911 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 22416892 | HCID 22416892 | — |
Reaction Steps
3-(7-trifluoromethyl-2-quinolinylmethoxy)aniline: 3.0 g of sodium carbonate are added to a solution of 2.0 g of 3-aminophenol in 200 ml of acetone and the mixture is stirred for 15 min. at 50°. 5.2 g of 2-bromomethyl-7-trifluoromethylquinoline, 6.1 g of caesium carbonate and 0.1 g of potassium iodide are added thereto and boiling under reflux is carried out for 2 hours. The reaction mixture is filtered, the precipitate is washed with acetone and the filtrate is concentrated by evaporation. The residue is taken up in hexane/ethyl acetate 3:2 and filtered over silica gel. The filtrate is concentrated by evaporation and the resulting oil is chromatographed on 400 g of silica gel using hexane/ethyl acetate 3:2. The title compound is obtained in the form of a yellow solid of m.p. 85°-86°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05508408 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-6e33bda317404099a1ec3d2f5b60a07a |
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| Source note | uspto-grants-1996_04 |
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