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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523116생성일: 2026년 10월 26일

1-Fluoro-3-iodobenzene → Tert-butyl 3-(3-fluorophenyl)prop-2-ynoate

https://huagongshe.com/reaction/523116

반응식

참여 물질

역할이름HCID투입량
반응물1-Fluoro-3-iodobenzeneHCID 70725—
반응물tert-Butyl propiolateHCID 543038—
반응물Magnesium ChlorideHCID 5360315—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
용매Ammonium ChlorideHCID 25517—
생성물Tert-butyl 3-(3-fluorophenyl)prop-2-ynoateHCID 8976081975%

반응 조건

온도25 °C

반응 단계

A dry, argon-filled Schlenk tube with a magnetic stirrer bar and septum is initially charged with tert-butyl prop-2-ynoate (70 mg, 0.56 mmol) in anhydrous THF (2 ml). After adding (TMP)2Zn.MgCl2 (2.2 ml, 1.2 mmol) at 25° C., the mixture is stirred for 30 min, then a solution of 1-fluoro-3-iodobenzene (160 mg, 0.72 mmol), tetrakis(triphenylphosphine)palladium(0) (33 mg, 5 mol %) in anhydrous THF (2 ml) is added dropwise and the mixture is stirred at 25° C. overnight. For workup, the mixture is diluted with aqueous sat. NH4Cl solution (30 ml) and extracted with ethyl acetate (3×30 ml). After the combined organic phases have been dried over Na2SO4, the solvent has been distilled off and purification has been effected by column chromatography on silica gel (heptane:ethyl acetate), the desired compound (91 mg, 75% of theory) was obtained as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334292B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-2ce4876180e64b929f40fda87d2399cc
출처 메모uspto-grants-2016_05