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HRID 429257作成日:2026年10月26日
Fipronil → 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(N-hydroxy-N-methylamidino)-4-trifluoromethylsulfinylpyrazole
https://huagongshe.com/reaction/429257
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Fipronil | HCID 3352 | — |
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | N-methylhydroxylamine hydrochloride | HCID 77906 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(N-hydroxy-N-methylamidino)-4-trifluoromethylsulfinylpyrazole | HCID 11070934 | 53% |
反応手順
5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinylpyrazol e (1.00 g, 2.29 mmol) was dissolved in 10 ml of 1,4-dioxane and N-methylhydroxylamine hydrochloride (0.38 g, 4.55 mmol) and triethylamine (0.65 ml, 4.68 mmol) were added, and then the mixture was stirred at room temperature for 3 hours. After 30 ml of water, 60 ml of ethyl acetate and 30 ml of an aqueous saturated sodium chloride solution were added, the reaction mixture was shaken and the ethyl acetate layer was taken. The ethyl acetate layer was washed twice with 50 ml of water and dried over anhydrous magnesium sulfate and the solvent was distilled off to obtain a crystal. This crystal was washed with chloroform and then recrystallized from ethanol-hexane to obtain 0.59 g (1.22 mmol) of the title compound as a colorless crystal. Yield 53%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06316477B1 |
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| 出典データセット | uspto-grants-2001_11 |
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| ORD ID | ord-7bd5b7d0393c4059ac4c3f2448cc035e |
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| 出典メモ | uspto-grants-2001_11 |
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