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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426290Generated: November 2, 2026

Methyl iodide → Benzoic acid, 3-fluoro-5-methyl-, methyl ester

https://huagongshe.com/reaction/1426290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-5-methylbenzoic acidHCID 2778447—
SolventAcetoneHCID 180—
ProductBenzoic acid, 3-fluoro-5-methyl-, methyl esterHCID 44203100—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 3-fluoro-5-methylbenzoic acid (1.50 g, 9.73 mmol, Oakwood) in Acetone (40 mL) was added Potassium carbonate (1.34 g, 9.73 mmol) followed by Methyl iodide (0.73 mL, 12 mmol). The reaction mixture was heated to 65° C. for 1 hour, heating discontinued and stirred overnight, then heating resumed at that temperature for a further 2 hours. Additional Methyl iodide (0.5 mL, 8 mmol) was added and heating was continued for 6 hours. Solids were removed by filtration and acetone was removed in vacuo. The residue was partitioned between 1N NaOH and ethyl acetate. The aqueous portion was extracted with a further two portions of ethyl acetate. The combined extracts were washed with brine, then dried over sodium sulfate, decanted and concentrated. The product so obtained was used without further purification (1.64 g, 100%). 1H NMR (300 MHz, CDCl3): δ 7.66-7.63 (m, 1H), 7.51 (d, 1H), 7.10-7.04 (m, 1H), 3.91 (s, 3H), 2.40 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933085B2
Source datasetuspto-grants-2015_01
ORD IDord-2ea7cfbc03cd41209ab6f140629df780
Source noteuspto-grants-2015_01