Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 86644483 | HCID 86644483 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86644482 | HCID 86644482 | 94% |
Reaction Steps
1.1 g of ethyl 1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}-3-{1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy}pyrazole-5-carboxylate was dissolved in 30 mL of toluene, followed by cooling to −78° C., and 2.6 mL of a toluene solution (1.0 mol/L) of diisobutyl aluminum hydride was slowly dropwise added. After stirring for 3 hours, a saturated aqueous solution of ammonium chloride was added, extraction with ethyl acetate was carried out, the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and the obtained residue was purified by column chromatography (developing solvent ethyl acetate:hexane=1:3) to obtain 0.95 g of 5-formyl-1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}-3-{1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy}pyrazole (1H-NMR (CDCL3/TMS δ (ppm) value) δ: 2.56 (3H, s), 3.39 (2H, q), 6.05 (1H, dt), 6.85 (1H, s), 7.17 (1H, d), 7.66 (1H, d), 9.72 (1H, d)).
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-8d6b99e9af6b40c1ab16a8d5daa9b884 |
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| Source note | uspto-grants-2014_08 |
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