Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 66899696 | HCID 66899696 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69218892 | HCID 69218892 | — |
Reaction Steps
3-[3-(2-Butoxy-3,5-diisopropyl-phenyl)-1H-indol-5-yl]-but-2-enoic acid (129 mg, 0.30 mmol), cesium carbonate (293 mg, 0.90 mmol), and iodomethane (0.041 mL, 65 mmol) were combined in DMF (6 mL) and heated at 40° C. for 2 h. The reaction was diluted with water and extracted with ethyl acetate (2×). The organic portions were combined and washed with brine, dried (MgSO4), filtered and concentrated in vacuo to provide 139 mg of a yellow oil. The material was purified using radial chromatography by elution with (95:5) hexane:ethyl acetate to provide 119 mg (86%) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348359B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-30d19c70cb7b4d46a3ea47b06644e66b |
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| Source note | uspto-grants-2008_03 |
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