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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419621Generated: October 24, 2026

Iodoethane → 1-Ethoxy-5-fluoro-4-methyl-2-nitrobenzene

https://huagongshe.com/en/reaction/419621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-4-methyl-2-nitrophenolHCID 12782411—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product1-Ethoxy-5-fluoro-4-methyl-2-nitrobenzeneHCID 5945288360.6%

Reaction Steps

4-Methyl-5-fluoro-2-nitrophenol (11.1 g, 65.0 mmol) and iodoethane (12.2 g, 78.0 mmol) were dissolved in 100 mL of DMSO with stirring. K2CO3 (13.5 g, 97.5 mmol) was added. The reaction was stirred for 3 h and then diluted with DCM and filtered. The filtrate was poured into H2O and extracted with DCM. The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo to provide the title compound of step A (8.0 g, 39.4 mmol) as a pale yellow crystalline solid. 1H NMR (400 MHz, CDCl3) δ 7.76 (d, J=8.1 Hz, 1H), 6.70 (d, J=11.0 Hz, 1H), 4.10 (q, J=7.0 Hz, 2H), 2.22 (s, 3H), 1.45 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-f8596cf6d2564e7abe2e4f04878f3b32
Source noteuspto-grants-2012_01