Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Iodophenol | HCID 12272 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-Iodophenoxy)-1,3-thiazole | HCID 60753841 | 72.3% |
Reaction Steps
Cesium carbonate (4.52 g, 13.87 mmol) was added to 2-bromo-1,3-thiazole (1.90 g, 11.6 mmol) and 3-iodophenol (2.54 g, 11.5 mmol) in anhydrous DMF (30 mL). The reaction was heated to 135° C. and stirred at this temperature overnight. The reaction was allowed to cool, then was poured into water (100 mL), and extracted with EtOAc (3×100 mL). The combined organics were washed with brine (100 mL), dried (MgSO4), filtered, and concentrated. The crude product was purified via flash chromatography using a Varian SF15-24 g column and an eluent of EtOAc in hexanes (0-10%) to afford the title compound as a yellow oil (2.52 g, 71.8%). MS (LCMS) m/z 304.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08624034B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-e11f655efc1849be8f6ecd15874ae1b8 |
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| Source note | uspto-grants-2014_01 |
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