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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499902Generated: November 3, 2026

Iodoethane → 4-Acetyl-3-ethoxy-2-iodo-6-methylbenzonitrile

https://huagongshe.com/reaction/1499902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86677824HCID 86677824—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Acetyl-3-ethoxy-2-iodo-6-methylbenzonitrileHCID 8667782596%

Reaction Conditions

Temperature60 °C

Reaction Steps

The 4-acetyl-3-hydroxy-2-iodo-6-methylbenzonitrile (5.0 g, 17 mmol) was dissolved in N,N-dimethylformamide (50.0 mL) and the potassium carbonate (4.6 g, 33 mmol) and ethyl iodide (2.1 mL, 33 mmol) were added. The reaction was heated to 60° C. and monitored by LC/MS. After heating for 2 hrs the reaction was complete. This was allowed to cool, diluted with ethyl acetate (300 mL) and filtered to remove the remaining solids. The organic layer was washed with water (3×), brine, dried over magnesium sulfate and concentrated to give the crude product as a dark solid. The product was purified by FCC on silica gel eluting hexane:ethyl acetate gradient to give 4-acetyl-3-ethoxy-2-iodo-6-methylbenzonitrile as a pale yellow crystalline solid (5.0 g, 96%). LCMS calculated for C12H13INO2 (M+H)+: m/z=329.9; found: 330.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199982B2
Source datasetuspto-grants-2015_12
ORD IDord-0638e4c8d86747069470eaa66da65ab6
Source noteuspto-grants-2015_12