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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419567Generated: October 25, 2026

Water → 1-Ethyl-2-fluoro-4-methoxy-5-nitrobenzene

https://huagongshe.com/reaction/419567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 59452993HCID 59452993—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product1-Ethyl-2-fluoro-4-methoxy-5-nitrobenzeneHCID 5945284783.4%

Reaction Steps

4-Ethyl-5-fluoro-2-nitrophenol (5.72 g, 30.9 mmol) was dissolved in 60 mL of DMSO with stirring. K2CO3 (6.41 g, 46.4 mmol) was added. Methyl iodide (2.5 mL, 40 mmol) was added via syringe. The reaction was stirred overnight and poured into H2O and diethyl ether. The layers were separated, and the organic layer was washed with brine. The combined aqueous layers were extracted with EtOAc (2×). The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by flash chromatography to afford 5.13 g (83%) of the title compound of step C. 1H NMR (400 MHz, DMSO-d6) δ 7.88 (d, J=7.9 Hz, 1H), 7.23 (d, J=12.1 Hz, 1H), 3.86 (s, 3H), 2.56 (q, J=7.6 Hz, 2H), 1.11 (t, J=7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-2096705a56624efe8fbc1b323e23098a
Source noteuspto-grants-2012_01