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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738303Generated: November 2, 2026

Methyl iodide → 5-(4-Fluorobenzoyl)-6-methoxy-2-methylsulfonylnaphthalene

https://huagongshe.com/reaction/1738303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15434620HCID 15434620—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(4-Fluorobenzoyl)-6-methoxy-2-methylsulfonylnaphthaleneHCID 1543461696.2%

Reaction Steps

A mixture of 5-(4-fluorobenzoyl)-6-hydroxy-2-methylsulfonylnaphthalene (1.0 g, 2.9 mmol), [prepared as described in step 3 above], methyl iodide (0.65 ml, 10.45 mmol), and potassium carbonate (0.64 g, 4.65 mmol) in N,N-dimethylformamide (10 ml) was stirred at room temperature. After 16 h, the reaction mixture was diluted with water and extracted into ethyl acetate. The organic layer was separated, washed with brine, and dried over sodium sulfate. The solvent was removed in vacuo and the crude product was purified by flash chromatography (gradient elution 40-100% ethyl acetate/hexanes) to give 1.0 g of 5-(4-fluorobenzoyl)-6-methoxy-2-methylsulfonylnaphthalene as a solid (96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962531
Source datasetuspto-grants-1999_10
ORD IDord-7abdb5db2bbd424a82693cc871c81142
Source noteuspto-grants-1999_10