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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095006Generated: October 31, 2026

Methyl iodide → Methyl 5-methoxy-2-nitrobenzoate

https://huagongshe.com/reaction/1095006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Methoxy-2-nitrobenzoic acidHCID 339209—
SolventDimethylformamideHCID 6228—
SolventEthyl 2-amino-4,5-bis(2-methoxyethoxy)benzoateHCID 11347513—
ProductMethyl 5-methoxy-2-nitrobenzoateHCID 12719167100.8%

Reaction Steps

5-Methoxy-2-nitro-benzoic acid (2.5 g) was dissolved in N,N-dimethylformamide (compound A′) (40 ml). Potassium carbonate (4.5 g) and methyl iodide (2.5 ml) were added to the solution at room temperature, and the mixture was then stirred at that temperature for 30 min. After the completion of the reaction, distilled water was added thereto at room temperature, and the mixture was then subjected to separatory extraction with ethyl acetate. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated under the reduced pressure. The residue was purified by column chromatography eluted with a hexane-acetone system to give 5-methoxy-2-nitrobenzoic acid methyl ester (2.7 g, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-66c74d10c9cf484288d2a53e3b2a5b85
Source noteuspto-grants-2012_03