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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 269982생성일: 2026년 10월 27일

1-Iodo-4-nitrobenzene → p-Allylnitrobenzene

https://huagongshe.com/reaction/269982

반응식

참여 물질

역할이름HCID투입량
반응물1-Iodo-4-nitrobenzeneHCID 12495—
반응물AllyltributylstannaneHCID 90628—
반응물Potassium FluorideHCID 522689—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매Diethyl EtherHCID 3283—
용매1,4-DioxaneHCID 31275—
생성물p-AllylnitrobenzeneHCID 59595355%

반응 단계

Add allyl tri-n-butylstannane (30.10 mmol, 9.33 ml) dropwise to a stirred solution of 4-iodo-nitrobenzene (5 g, 20.07 mmol), tetrakis-(triphenylphosphine) palladium(0) (1.16 g, 1 mmol) and copper (I) iodide (306 mg, 1.6 mmol) in 50 ml of dry 1,4-dioxane under argon atmosphere. Reflux the mixture for 24 hours and then cool to room temperature. Dilute the solution with 40 ml of diethyl ether and add 20 ml of saturated solution of KF and stir for 2 hours. Filter the mixture and wash the organic layer with water (20 ml), brine (20 ml) and dry over sodium sulfate. Evaporate the solution under reduced pressure and purify the residue by flash chromatography on silica gel using hexane-ethyl acetate as eluent (20:1) to afford 1.80 g (55%) of 1-allyl-4-nitrobenzene. Add a solution of 3-chloro-peroxybenzoic acid (5.98 g, 24.28 mmol), in 20 ml of dichloromethane to a solution of 1-allyl-4-nitro-benzene (1.8 g, 11.04 mmol) in 50 ml of dichloromethane and stir the mixture at room temperature overnight. Quench with saturated NaHCO3 (15 ml), and wash the organic layer three times with saturated NaHCO3 and dry over magnesium sulfate. Evaporate under reduced pressure to afford 1.4 g (71%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449477B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-eb64e9e5d5d0411b9bee90b4279b0e0e
출처 메모uspto-grants-2008_11