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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404532Generated: October 30, 2026

HCID 86644461, compound → HCID 86644460, compound

https://huagongshe.com/reaction/2404532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86644461HCID 86644461—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 86644460HCID 8664446090.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

Then, 4.5 g of 5-acetylamino-1-(2-fluoro-4-methyl-5-methylsulfinylphenyl)-3-(2,2,3,3,3-pentafluoropropoxy)pyrazole was dissolved in 200 mL of acetic anhydride, followed by stirring at 120° C. for 6 hours. Acetic anhydride was distilled off under reduced pressure, the obtained residue was dissolved in 150 mL of ethanol, and 4.0 g of potassium carbonate was added, followed by stirring at room temperature for 12hours. Neutralization with a 6N hydrochloric acid aqueous solution was carried out, and 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 silica gel column chromatography (developing solvent ethyl acetate:hexane=1:4) to obtain 3.8 g of 5-acetylamino-1-(2-fluoro-4-methyl-5-mercaptophenyl)-3-(2,2,3,3,3-pentafluoropropoxy)pyrazole (1H-NMR (CDCL3/TMS δ (ppm) value) δ: 2.09 (3H, s), 2.38 (3H, s), 3.39 (1H, s), 4.66 (2H, t), 6.20 (1H, s), 7.09 (1H, d), 7.14 (1H, brs), 7.39 (1H, d)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802713B2
Source datasetuspto-grants-2014_08
ORD IDord-e45a0dfc72d14edd9ac05449bf8a810c
Source noteuspto-grants-2014_08