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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10229Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Methylbenzo[b]thiopheneHCID 73817—
EduktSelectfluorHCID 2724933—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-Fluoro-3-methyl-1-benzothiopheneHCID 2197837172%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094777B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-25fc685f89c34fc6805c7197facceebe
Quellennotizuspto-grants-2006_08