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HRID 375810생성일: 2026년 10월 23일

2-Bromo-4-methylaniline → (2-Bbromo-4-methylphenyl)hydrazine hydrochloride

https://huagongshe.com/ko/reaction/375810

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-4-methylanilineHCID 11422—
반응물Sodium NitriteHCID 23668193—
반응물Tin chloride monohydrateHCID 45051637—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물(2-Bbromo-4-methylphenyl)hydrazine hydrochlorideHCID 1649524881.1%

반응 단계

To a stirred, cooled (-5° C. solution of 2-bromo-4-methyl-aniline (50.54 g, 0.272 mol) in concentrated HCl solution (200 mL) was added sodium nitrite (18.9 g, 0.274 mol) in water (200 mL) dropwise at such a rate as to maintain temperature below 5° C. After complete addition, the mixture was further stirred[at 5° C. for 30 minutes. A solution of tin chloride monohydrate (185.4 g, 0.822 mol) in concentrated HCl (total volume 400 mL) was added dropwise again maintaining temperature below 5° C. After complete addition and 30 minutes of further stirring, the mixture was placed in the freezer overnight. The light brown solid which precipitated was isolated by filtration and washed with cold brine followed by a solution of petroleum ether/diethyl ether (2/1 by volume). This solid was slowly added to an ice cooled mixture of 50% sodium hydroxide solution/ethyl acetate. The mixture was extracted with ethyl acetate and the organic phase dried over magnesium sulfate. After filtration, the solution was concentrated to 400 mL total volume, diluted with diethyl ether (1.5 L) and treated with dry HCl. The product, 2-bromo-4-methyl-phenylhydrazine hydrochloride (52.4 g) was isolated as a light brown solid and used without further purification. ##STR37##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05488053
출처 데이터셋uspto-grants-1996_01
ORD IDord-14b724ca69204e9ead44129dd3bfaf4f
출처 메모uspto-grants-1996_01