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HRID 1410289생성일: 2026년 10월 27일

Trifluoromethanesulfonic acid → 5-Bromo-2-chloro-4-hydroxybenzonitrile

https://huagongshe.com/reaction/1410289

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물N-bromobutanimideHCID 67184—
반응물2-Chloro-4-hydroxybenzonitrileHCID 592797—
용매AcetonitrileHCID 6342—
생성물5-Bromo-2-chloro-4-hydroxybenzonitrileHCID 5333045286.2%

반응 조건

온도-30 °C

반응 단계

To a solution of 2-chloro-4-hydroxybenzonitrile (1, 10 g, 65 mmol) in acetonitrile (200 mL) at −30° C. was added dropwise trifluoromethanesulfonic acid (10 mL, 71 mmol). The solution was stirred for 10 min at −30° C., before adding of N-bromosuccinimide (16.2 g, 91 mmol). After 18 h stirring at ambient temperature, the solution was quenched with aqueous saturated sodium hydrogen carbonate. The organic layer was extracted with ethyl acetate two times, washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The resulting crude residue was purified on a Biotage® purification apparatus (silica gel, 5 to 40% ethyl acetate in hexanes gradient) to yield the title compound (13 g, 56 mmol, 86%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921412B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-bdb96887be414759b7e4176e6b8059c1
출처 메모uspto-grants-2014_12