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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56146생성일: 2026년 10월 24일

Dihexylamine → 2-fluoro-N,N-di-n-hexyl-4-nitroaniline

https://huagongshe.com/ko/reaction/56146

반응식

참여 물질

역할이름HCID투입량
반응물DihexylamineHCID 8920—
반응물Potassium CarbonateHCID 11430—
반응물1,2-Difluoro-4-nitrobenzeneHCID 123053—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물2-fluoro-N,N-di-n-hexyl-4-nitroanilineHCID 9002414586%

반응 조건

온도90 °C

반응 단계

To a solution of 3,4-difluoronitrobenzene (1.59 g, 10 mmol) in DMSO (15 mL) were added K2CO3 (3.04 g, 22 mmol) and di-n-hexylamine (2.04 g, 11 mmol). The mixture was heated at 90° C. overnight, then cooled to rt, diluted with water (50 mL) and extracted with CH2Cl2 (50 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/CH2Cl2 (V/V)=10:1) to give the title compound as pale yellow oil (2.79 g, 86%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434695B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ba52dcdca5224e56bb6328da85a7e25d
출처 메모uspto-grants-2016_09