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HRID 257371作成日:2026年10月25日

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

https://huagongshe.com/reaction/257371

反応式

関与物質

役割名称HCID仕込み量
反応物Stannous chloride dihydrateHCID 61436—
反応物2-Fluoro-4-methoxyanilineHCID 3756383—
反応物Sodium NitriteHCID 23668193—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
生成物(2-Fluoro-4-methoxyphenyl)hydrazineHCID 44203045—

反応条件

温度-10 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262390
出典データセットuspto-grants-1993_11
ORD IDord-028c3e81b0304dad801bb50f136c649f
出典メモuspto-grants-1993_11