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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83487생성일: 2026년 10월 25일

Sodium Hydroxide → 1-phenyl-1H-pyrazol-3-amine

https://huagongshe.com/reaction/83487

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물3-Amino-1-phenylpyrazoleHCID 98736—
용매DimethylformamideHCID 6228—
용매1,4-DioxaneHCID 31275—
생성물1-phenyl-1H-pyrazol-3-amineHCID 59432024.7%

반응 단계

To a solution of 1-phenyl-4,5-dihydro-1H-pyrazol-3-ylamine (50.0 g) in N,N-dimethylformamide (150 ml) and 1,4-dioxane (500 ml) was added 3,4,5,6-tetrachloro-1,4-benzoquinone (84.0 g) under ice-cooling over 20 minutes, and the mixture was stirred at room temperature for 4.5 hours. To the reaction mixture was added a 2M aqueous solution of sodium hydroxide (400 ml) under ice-cooling over 25 minutes, and the mixture was stirred at room temperature for 1 hour. The mixture was filtered through Celite to remove the insoluble substance, and eluted with ethyl acetate (250 ml×3), and then the filtrate was extracted with ethyl acetate (300 ml). The resulting organic layer was sequentially washed with water (300 ml) and a saturated aqueous solution of sodium chloride (300 ml). The separated aqueous layer was extracted twice with ethyl acetate (300 ml). To the combined organic layer were added anhydrous sodium sulfate (50 g) and silica gel (50 g), and the mixture was stirred at room temperature for 1 hour. This mixture was filtered with silica gel (100 g) on Celite, and subjected to elution with ethyl acetate (250 ml×3). The filtrate was concentrated, and diisopropyl ether (500 ml) was added to the resulting residue, and the mixture was stirred at room temperature. The insoluble substance was collected by filtration, washed twice with diisopropyl ether (100 ml), and dried under reduced pressure to give the titled compound (12.2 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846746B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ee0a9341e31844ca894c4e17be8be2f9
출처 메모uspto-grants-2014_09