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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10229Generated: October 27, 2026

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

https://huagongshe.com/reaction/10229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylbenzo[b]thiopheneHCID 73817—
ReactantSelectfluorHCID 2724933—
SolventAcetonitrileHCID 6342—
Product2-Fluoro-3-methyl-1-benzothiopheneHCID 2197837172%

Reaction Conditions

Temperature70 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094777B2
Source datasetuspto-grants-2006_08
ORD IDord-25fc685f89c34fc6805c7197facceebe
Source noteuspto-grants-2006_08