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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17649생성일: 2026년 10월 24일

4-tert-Butylphenol → 2-n-Butylamino-4-(4-t-butylphenoxy)nitrobenzene

https://huagongshe.com/ko/reaction/17649

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-ButylphenolHCID 7393—
반응물Potassium CarbonateHCID 11430—
반응물N-butyl-5-fluoro-2-nitroanilineHCID 59566264—
용매DimethylformamideHCID 6228—
생성물2-n-Butylamino-4-(4-t-butylphenoxy)nitrobenzeneHCID 66977422—

반응 조건

온도90 °C

반응 단계

A mixture of 2-n-butylamino-4-fluoronitrobenzene (10 mmol), 4-t-butylphenol (13 mmol), solid K2CO3 (30 mmol) and DMF (30 mL) was heated with stirring at 90° C. for 10 h. The reaction was quenched by cold H2O (50 mL), and the resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with brine (2×50 mL) and dried (anhydrous Na2SO4). The solvent was removed in vacuo, and the crude products were purified by silica gel column chromatography (eluting with 10% EtOAc in hexane), giving 2-n-butylamino-4-(4-t-butylphenoxy)nitrobenzene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737285B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0b8aca2fd88841b99fc0aa3fcbd77d96
출처 메모uspto-grants-2010_06