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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723672Generated: October 25, 2026

Methyl iodide → 4-Fluoro-N-methyl-N-[2-(5-methyl-furan-2-yl)-ethyl]-benzamide

https://huagongshe.com/reaction/723672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamideHCID 21874846—
SolventTetrahydrofuranHCID 8028—
Product4-Fluoro-N-methyl-N-[2-(5-methyl-furan-2-yl)-ethyl]-benzamideHCID 2187496284%

Reaction Steps

NaH (60% dispersion in oil, 65 mg, 1.63 mmol) was added portionwise to a solution of 4-fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamide (269 mg, 1.09 mmol, 237A) in THF (5 mL). After gas evolution ceased, iodomethane (0.14 mL, 2.18 mmol) was added drop-wise. Once HPLC analysis showed the reaction to be 50% complete, the mixture was concentrated under reduced pressure and resubjected to the above conditions. After all the starting material was consumed, H2O was added and the resulting mixture was extracted with EtOAc (2×5 mL). The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. Purification by flash chromatography on silica gel eluting with 20% acetone/CHCl3 gave 238 mg (84%) of compound 425A. HPLC: 98% at 2.94 min (retention time) (Phenomenex-prime S5-C18 column 4.6×50 mm eluting with 10–90% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z [M+H]=262.38.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141578B2
Source datasetuspto-grants-2006_11
ORD IDord-b3934f16316f48639f3ea9f7a704bd0a
Source noteuspto-grants-2006_11