Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ammonium cerium-nitrate | HCID 57418452 | — |
| Reactant | HCID 68709923 | HCID 68709923 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68706611 | HCID 68706611 | 161.1% |
Reaction Steps
To a well stirred solution of 2.79 g of 5-(4-Fluoro-phenyl)-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester in 100 ml of Acetonitrile were added 1.71 g of Iodine and 3.70 g of Cerium ammonium nitrate. The mixture was stirred for 3 h at 50° C. The red solution was then allowed to cool and was concentrated in vaccuo. The residue was taken up in 200 ml of Ethyl acetate. The organic phase was successively washed with 5% Sodium bisulfite solution and brine. After drying over Magnesium sulfate and concentration, a beige solid 4.06 g (96%) was obtained which is sufficiently pure and was directly used in the next step. MS: m/e=375.3 ([M+1]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293916B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-e5ffa86961344987a6fcd4b75e9d78e2 |
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| Source note | uspto-grants-2012_10 |
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