Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Propanedioyl dichloride | HCID 74269 | — |
| Reactant | HCID 66842008 | HCID 66842008 | — |
| Product | HCID 178493574 | HCID 178493574 | — |
Reaction Steps
1.5 g of 2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenylhydrazine was dissolved in 70 mL of tetrahydrofuran, and 0.83 g of malonyl chloride was added under cooling with ice. Stirring was carried out under reflux with heating for 5 hours, and the solvent was distilled off under reduced pressure. To the obtained residue, 20 mL of dichloromethane and 2 mL of methanol were added, and 0.7 mL of a diethyl ether solution (2.0 mol/L) of trimethylsilyldiazomethane was added under cooling with ice, followed by stirring at room temperature for 5 hours. Then, the solvent was distilled off under reduced pressure, and the obtained residue was purified by column chromatography (developing solvent ethyl acetate:hexane=1:1) to obtain 0.14 g of 1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}-5-hydroxy-3-methoxypyrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802713B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-8f03ea9d8dfb495ca4bc3c2c37f73996 |
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| Source note | uspto-grants-2014_08 |
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