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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629188Generated: October 30, 2026

Hydrochloric Acid → 1-(2-Methoxy-3-nitrophenyl)ethanone

https://huagongshe.com/reaction/629188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Hydroxy-3-nitrophenyl)-ethanoneHCID 270026—
SolventDimethylformamideHCID 6228—
Product1-(2-Methoxy-3-nitrophenyl)ethanoneHCID 1557947197.5%

Reaction Steps

A slurry of 1-(2-hydroxy-3-nitrophenyl)ethanone (1.00 g, 5.52 mmol) and potassium carbonate (3.05 g, 22.08 mmol) in DMF (20 mL) was stirred at room temperature for 30 minutes, then iodomethane (1.338 mL, 16.56 mmol) was added dropwise and the resulting mixture was allowed to stir at room temperature overnight. LCMS indicated some un-reacted starting material remained, therefore additional iodomethane (1.338 mL, 16.56 mmol) was added and the mixture was warmed to 50° C. over 2 days. Reaction was quenched by the addition of water to give a solution followed by adjusting the pH with 1N HCl to ˜7. The resulting solution was extracted with ethyl acetate (80 mL×3) and the combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to afford the product, 1-(2-methoxy-3-nitrophenyl)ethanone (1.05 g, 5.38 mmol, 97% yield) as a tan oil. HPLC (Method N) RT=1.86 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315494B2
Source datasetuspto-grants-2016_04
ORD IDord-a8dc8e1cda124ce4bd4d084332cec486
Source noteuspto-grants-2016_04