戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1266922作成日:2026年10月26日

Hydrazine hydrate (1:1) → 2-Hydrazino-6-(4-trifluoromethylphenoxy)pyridine

https://huagongshe.com/reaction/1266922

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物2-Fluoro-6-(4-trifluoromethylphenoxy)pyridineHCID 18544783—
溶媒EthanolHCID 702—
生成物2-Hydrazino-6-(4-trifluoromethylphenoxy)pyridineHCID 1854478647.8%

反応条件

温度40 °C

反応手順

Next, a reaction flask was loaded with 2-fluoro-6-(4-trifluoromethylphenoxy)pyridine (8.0 g) and ethanol (60 ml), and heated up to 40° C. with stirring. To this mixture, hydrazine monohydrate (7.6 g) was dropwise added in 30 minutes. The temperature of the mixture was raised to the reflux temperature, followed by stirring for 20 hours. Thereafter, the heating was stopped, and the reaction mixture was cooled, followed by filtration to remove insoluble components. The filtrate was condensed by an evaporator to give 2-hydrazino-6-(4-trifluoromethylphenoxy)pyridine (4.0 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06551682B1
出典データセットuspto-grants-2003_04
ORD IDord-172563bbfa8c4f0e8db9a9212f308f10
出典メモuspto-grants-2003_04