Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ceric ammonium nitrate | HCID 180504 | — |
| Reactant | ethyl 1-methyl-1H-pyrazole-3-carboxylate | HCID 10582985 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178470493 | HCID 178470493 | 166% |
Reaction Steps
To a stirred solution of ethyl 1-methyl-1H-pyrazole-3-carboxylate (5 g, 32.4 mmol) in CH3CN (200 mL) under Ar was added I2 (4.94 g, 19.46 mmol) and after 5 min CAN (10.67 g, 19.46 mmol). The reaction mixture was stirred for 1 hr at 80° C., concentrated, quenched with a 10% aq. Na2S2O3 solution, and extracted with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4 and evaporated. The crude material was purified by silica gel column chromatography (hexane/EtOAc 25-45%) to afford the title product (9.04 g, 32.3 mmol, 100% yield) as a white solid. tR: 3.78 min (HPLC 1); tR: 0.80 min (LC-MS 2); ESI-MS: 281 [M+H]+ (LC-MS 2); Rf=0.45 (hexane/EtOAc 1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975417B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-e3da176e44e74702a863f1fbacbe075c |
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| Source note | uspto-grants-2015_03 |
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