戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 623708作成日:2026年10月24日

Pyridine → 2-(2,4-difluorophenyl)-4,5-dimethyl-2H-1,2,3-triazole 1-oxide

https://huagongshe.com/ja/reaction/623708

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2,4-Difluorophenylhydrazine hydrochlorideHCID 2733301—
反応物IsonitrosoacetoneHCID 6399095—
触媒Copper sulfate pentahydrateHCID 24463—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物2-(2,4-difluorophenyl)-4,5-dimethyl-2H-1,2,3-triazole 1-oxideHCID 90109810—

反応条件

温度23 °C

反応手順

To a stirred solution of anti-pyruvic aldehyde 1-oxime (2.2 g, 22.2 mmol) in diethyl ether (50 mL) was added 2,4-difluorophenylhydrazine hydrochloride (4.0 g, 22.2 mmol) and pyridine (2 mL). The reaction mixture was stirred at 23° C. for 64 h. The solid that formed was removed by filtration and washed with diethyl ether. The filtrate was concentrated under reduced pressure. The crude residue was dissolved in pyridine (100 mL). A solution of copper(II) sulfate pentahydrate (11.1 g, 44.4 mmol) in water (60 mL) was added at once and the resulting mixture was stirred at reflux for 20 h. The mixture was diluted with water and extracted with diethyl ether. The combined organic layers were washed with 1.0 M aqueous hydrochloric acid, dried (MgSO4) and concentrated under reduced pressure to afford the crude product. The crude material was purified by chromatography on silica gel eluting with 0 to 100% ethyl acetate in hexanes to obtain the title compound (1.98 g) as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09302999B2
出典データセットuspto-grants-2016_04
ORD IDord-8a8bc382c165408fb7cb9611391531c6
出典メモuspto-grants-2016_04