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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168506Generated: October 30, 2026

Methyl iodide → Methyl 5-fluoro-3-methyl-2-nitrobenzoate

https://huagongshe.com/reaction/2168506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant5-Fluoro-3-methyl-2-nitrobenzoic acidHCID 53430776—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-fluoro-3-methyl-2-nitrobenzoateHCID 5341516698.5%

Reaction Steps

To a solution of 5-fluoro-3-methyl-2-nitrobenzoic acid (8.0 g, 40 mmol) from Step A above in DMF (100 mL) was added cesium carbonate (20.0 g, 60 mmol) followed by iodomethane (3.0 ml, 48 mmol). The reaction solution was stirred at ambient temperature overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extract was separated, washed with brine, dried (Na2SO4), and concentrated in vacuo to afford methyl 5-fluoro-3-methyl-2-nitrobenzoate (8.4 g, 98%) as a yellow solid: 1H NMR (500 MHz, DMSO-d6) δ 7.71-7.67 (m, 2H), 3.85 (s, 3H), 2.32 (s, 3H); MS (ESI+) m/z 214 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045501B2
Source datasetuspto-grants-2015_06
ORD IDord-3a62075a991045459e4eadb72c8d17f2
Source noteuspto-grants-2015_06