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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37621생성일: 2026년 10월 24일

Water → 2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline

https://huagongshe.com/ko/reaction/37621

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물2-(4-[(2-Ethylquinolin-4-yloxy)methyl]phenyl)-5,5-dimethyl-1,3,2-dioxaborinaneHCID 19935772—
반응물5-(2-bromophenyl)-1-(4-nitrophenyl)-1H-tetrazoleHCID 19935790—
촉매HCID 178418397HCID 178418397—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinolineHCID 1993578458.2%

반응 조건

온도60 °C

반응 단계

A mixture of potassium carbonate (1.08 g; 7.8 mmol), 5-(2-bromophenyl)-1-(4-nitrophenyl)-1H-tetrazole (1.16 g; 3.2 mmol) (obtained as described in Procedure A, step (ii)), water (10 ml), toluene (10 ml), and methanol (10 ml) was heated to 60° C. to give a clear solution. Compound H (1.0 g; 2.6 mmol) and tetrakis(triphenylphosphine)palladium (0.06 g; 0.05 mmol) were added and the reaction mixture heated at reflux for 6 hours. The mixture was allowed to cool and further toluene (10 ml) added. The organic phase was separated and the aqueous phase extracted with toluene (2×20 ml). The combined organic phases were evaporated and the resultant solid recrystallised from toluene to give 2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline (A) as a solid (0.8 g); m.p. and NMR similar to that of the product of procedure A, part (v).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420292
출처 데이터셋uspto-grants-1995_05
ORD IDord-a169e26cbd7e456187a8e2d670e7201c
출처 메모uspto-grants-1995_05