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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404549Generated: October 29, 2026

Ammonium Chloride → HCID 86644482, compound

https://huagongshe.com/reaction/2404549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 86644483HCID 86644483—
SolventTolueneHCID 1140—
ProductHCID 86644482HCID 8664448294%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802713B2
Source datasetuspto-grants-2014_08
ORD IDord-8d6b99e9af6b40c1ab16a8d5daa9b884
Source noteuspto-grants-2014_08