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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1384202생성일: 2026년 10월 26일

Toluene → 4-Nitrophenyl 2-(4-isobutylphenyl)pyridine-3-sulphonate

https://huagongshe.com/reaction/1384202

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium FluorideHCID 522689—
반응물(4-Isobutylphenyl)boronic acidHCID 2773472—
반응물4-Nitrophenyl 2-chloropyridine-3-sulphonateHCID 21186255—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
생성물4-Nitrophenyl 2-(4-isobutylphenyl)pyridine-3-sulphonateHCID 2118622855.3%

반응 단계

Tetrakis(triphenylphosphine)palladium(0) (0.076 g) was added to a deoxygenated mixture of 4-nitrophenyl 2-chloropyridine-3-sulphonate (0.69 g), 4-isobutylphenylboronic acid (0.47 g), potassium fluoride (0.38 g), toluene (15 ml) and water (2.5 ml) and the mixture was stirred and heated under reflux for 24 hours. Water (50 ml) was added and the mixture was extracted with ethyl acetate (2×80 ml). The organic extracts were washed with saturated sodium chloride solution and then combined and dried (MgSO4). Volatile material was removed by evaporation and the residue was purified by gradient elution with dichloromethane/hexane (1:1-1:0 v/v) then dichloromethane/hexane/ethyl acetate (10:9:1 v/v) through a silica gel Mega Bond Elut column followed by recrystallisation from ethyl acetate/hexane to give 4-nitrophenyl 2-(4-isobutylphenyl)pyridine-3-sulphonate (0.50 g), m.p. 123-124° C.; 1H NMR (d6-DMSO): 0.9 (d, 6H), 1.9 (m, 1H), 2.55 (d, 2H), 7.2-7.3 (m, 4H), 7.5 (d, 2H), 7.7 (dd, 1H), 8.2 (d, 2H), 8.4 (dd, 1H), 9.0 (dd, 1H); mass spectrum (+ve FAB, NBA/DMSO): 413 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06258817B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-88689a5c7139437f89a0c28cb08a1090
출처 메모uspto-grants-2001_07