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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10229생성일: 2026년 10월 23일

3-Methylbenzo[b]thiophene → 2-Fluoro-3-methyl-1-benzothiophene

https://huagongshe.com/ko/reaction/10229

반응식

참여 물질

역할이름HCID투입량
반응물3-Methylbenzo[b]thiopheneHCID 73817—
반응물SelectfluorHCID 2724933—
용매AcetonitrileHCID 6342—
생성물2-Fluoro-3-methyl-1-benzothiopheneHCID 2197837172%

반응 조건

온도70 °C

반응 단계

A stirred solution of 3-methylbenzothiophene (0.51 g, 3.37 mmol) in acetonitrile (5 μL) under nitrogen was treated with SELECTFLUOR™ (1.25 g, 3.35 mmol) and heated to 70° C. overnight. The solvent was removed in vacuo. The residue was taken up in ethyl acetate and washed with sodium hydrogen carbonate solution, water and brine, dried over MgSO4 and evaporated in vacuo. Purification by flash column chromatography on silica, eluting with isohexane, gave 2-fluoro-3-methyl-1-benzothiophene (72% pure, 190 mg, 0.82 mmol) which was treated according to the method of Example 29 Step 2 to give 3-(bromomethyl)-2-fluoro-1-benzothiophene (95 mg, 12%). 1H NMR (500 MHz, CDCl3) δ 7.75 (1H, d, J=8.0 Hz), 7.68 (1H, d, J=8.0 Hz), 7.46 (1H, t, J=7.6 Hz), 7.39–7.35 (1H, m), 4.65 (2H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094777B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-25fc685f89c34fc6805c7197facceebe
출처 메모uspto-grants-2006_08