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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74003생성일: 2026년 10월 24일

Water → 2-Tert-butyl-4-(2-ethoxyphenyl)-5-nitrophenol

https://huagongshe.com/ko/reaction/74003

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물(2-Ethoxyphenyl)boronic acidHCID 2734902—
반응물2-Tert-butyl-4-bromo-5-nitrophenolHCID 57470236—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물2-Tert-butyl-4-(2-ethoxyphenyl)-5-nitrophenolHCID 5747024097.2%

반응 조건

온도90 °C

반응 단계

To a solution of 2-tert-butyl-4-bromo-5-nitrophenol (C-14-a) (8.22 g, 30 mmol) in DMF (90 mL) was added 2-ethoxyphenyl boronic acid (5.48 g, 33 mmol), potassium carbonate (4.56 g, 33 mmol), water (10 ml) and Pd(PPh3)4 (1.73 g, 1.5 mmol). The mixture was heated at 90° C. for 3 h under nitrogen. The solvent was removed under reduced pressure. The residue was partitioned between water and ethyl acetate. The combined organic layers were washed with water and brine, dried and purified by column chromatography (petroleum ether-ethyl acetate, 10:1) to afford 2-tert-butyl-4-(2-ethoxyphenyl)-5-nitrophenol (9.2 g, 92%). 1H NMR (DMSO-d6) δ 10.38 (s, 1H), 7.36 (s, 1H), 7.28 (m, 2H), 7.08 (s, 1H), 6.99 (t, 1H, J=7.35 Hz), 6.92 (d, 1H, J=8.1 Hz), 3.84 (q, 2H, J=6.6 Hz), 1.35 (s, 9H), 1.09 (t, 3H, J=6.6 Hz); ESI-MS 314.3 m/z (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829204B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6cb6e0d7921243efbb85a3795c2e1928
출처 메모uspto-grants-2014_09