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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51432생성일: 2026년 10월 23일

Sodium Carbonate → 2-Carbomethoxy-6-nitro-2'-methoxy-biphenyl

https://huagongshe.com/ko/reaction/51432

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Methoxyphenylboronic acidHCID 2733958—
반응물Methyl 2-chloro-3-nitrobenzoateHCID 10751184—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
용매AluminumHCID 5359268—
생성물2-Carbomethoxy-6-nitro-2'-methoxy-biphenylHCID 2274044369.5%

반응 단계

A solution of methyl 2-chloro-3-nitrobenzoate (2.16 g, 10.0 mM), 2-methoxybenzeneboronic acid (1.64 g, 10.5 mM), tetrakis(triphenylphosphine)palladium (0) (584 mg, 0.5 mM), and 2 M aqueous sodium carbonate (10.5 mL, 21.0 mM) in 50 mL of THF was wrapped in aluminum foil and stirred at reflux for 27 hours. The THF was removed in vacuo and the residue dissolved in ethyl acetate. The mixture was washed with with H2O, 1 N HCl, H2O, sat. NaHCO3, and saturated brine, dried over magnesium sulfate, filtered, and concentrated. The resultant light brown oil was purified by column chromatography on silica (elution with gradient toluene/ethyl acetate) to afford 2.0 g (69%) of 2-carbomethoxy-6-nitro-2′-methoxy-biphenyl as a yellow-orange solid. 1H NMR (CDCl3) δ8.05 (d, 1H, J=8 Hz), 7.95 (d, 1H, J=8 Hz), 7.55 (t, 1H, J=8 Hz), 7.35 (t, 1H, J=8 Hz), 7.05 (d, 1H, J=8 Hz), 7.0 (t, 1H, J=8 Hz), 6.9 (d, 1H, J=8 Hz), 3.7 (s, 3H), and 3.6 (s, 3H). IR (KBr, cm−1) 1730, 1538, 1499, 1366, 1298, 1271, 1130, 774, 765, 759, 752, and 707. MS (ES) m/e 288.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713645B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-4c59ee4e2d2b4b46a25e5b6e76fcd145
출처 메모uspto-grants-2004_03