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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1266922생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1266922

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물2-Fluoro-6-(4-trifluoromethylphenoxy)pyridineHCID 18544783—
용매EthanolHCID 702—
생성물2-Hydrazino-6-(4-trifluoromethylphenoxy)pyridineHCID 1854478647.8%

반응 조건

온도40 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06551682B1
출처 데이터셋uspto-grants-2003_04
ORD IDord-172563bbfa8c4f0e8db9a9212f308f10
출처 메모uspto-grants-2003_04