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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257371생성일: 2026년 10월 26일

Stannous chloride dihydrate → (2-Fluoro-4-methoxyphenyl)hydrazine

https://huagongshe.com/reaction/257371

반응식

참여 물질

역할이름HCID투입량
반응물Stannous chloride dihydrateHCID 61436—
반응물2-Fluoro-4-methoxyanilineHCID 3756383—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물(2-Fluoro-4-methoxyphenyl)hydrazineHCID 44203045—

반응 조건

온도-10 °C

반응 단계

With vigorous stirring, 9.15 g (0.065 mole) of 2-fluoro-4-methoxyaniline (Example 3, Step B) was added to 60 mL of concentrated hydrochloric acid that had been cooled to -10° C. A solution of 4.83 g (0.070 mole) of sodium nitrite in 30 mL of water was slowly added dropwise, while the temperature was kept at or below -10° C. Upon completion of addition, the reaction mixture was stirred at -10° C. for one hour, after which 33.85 (0.150 mole) of tin(II) chloride dihydrate in 50 mL of concentrated hydrochloric acid Was added slowly, dropwise, while the temperature was kept below -5° C. After the reaction mixture had stirred for one hour as it warmed to ambient temperature, the crude product was filtered from the mixture and dissolved in 250 mL of water. This solution was made basic with 4N sodium hydroxide and extracted with methylene chloride. The combined extracts were dried over anhydrous sodium sulfate and filtered. The filtrate was placed on a silica gel column and eluted with methylene chloride to remove colored impurities and then with ethyl acetate to obtain the desired product. The solvent was evaporated under reduced pressure to yield 6.30 g of 2-fluoro-4-methoxyphenylhydrazine. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262390
출처 데이터셋uspto-grants-1993_11
ORD IDord-028c3e81b0304dad801bb50f136c649f
출처 메모uspto-grants-1993_11