戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 523459作成日:2026年10月26日

Water → 3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-fluoromethyl-4-trifluoromethylthiopyrazole

https://huagongshe.com/reaction/523459

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sulfur, trifluoro(N-methylmethanaminato)-HCID 123203—
反応物3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-hydroxymethyl-4-trifluoromethylthiopyrazoleHCID 9803048—
溶媒DichloromethaneHCID 6344—
生成物3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-fluoromethyl-4-trifluoromethylthiopyrazoleHCID 2478546784%

反応手順

Dimethylaminosulfur trifluoride (2.27 mL) was added to a solution of 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-hydroxymethyl-4-trifluoromethylthiopyrazole (2.9 g) in dichloromethane. After stirring for 3 hours, water was added followed by dichloromethane. The organic phase was washed with an aqueous solution of saturated sodium bicarbonate, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give a residue that was purified by chromatography (SiO2, heptane/EA) to afford the title compound as a white solid (2.45 g, 84%). 1H NMR: (400 MHz, CDCl3): 5.38 (d, J=47.5 Hz, 2H) and 7.83 (s, 2H). 19F NMR (376 MHz, CDCl3): −43.83 (s, 3F), −63.76 (s, 3F) and −84.12 (t, J=47.5 Hz, 1F).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09339033B2
出典データセットuspto-grants-2016_05
ORD IDord-1be2f41ed8c142d08df7f1bb14763d3d
出典メモuspto-grants-2016_05