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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921309Generated: November 4, 2026

Potassium Iodide → 5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1921309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant5-(5-Ethyl-6-methoxy-2-methylpyridin-3-yl)thiophene-2-carbaldehydeHCID 11521776—
SolventAcetonitrileHCID 6342—
Product5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-carbaldehydeHCID 58808543167.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 5-(5-ethyl-6-methoxy-2-methylpyridin-3-yl)thiophene-2-carbaldehyde (0.7 g, 2.9 mmol) prepared in accordance with the procedures of Step 2 as described above, potassium iodide (1.43 g, 8.6 mmol) and acetonitrile (15 mL) is added chlorotrimethylsilane (1.1 mL, 8.6 mmol) at room temperature then the reaction is heated at 60° C. for 0.5 hr. Solid product begins to form so more solvent is added to facilitate stirring. The solids are collected by filtration, washed with water, with ether and dried to afford 5-(5-ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-carbaldehyde (1.2 g, 61% yield). MS: m/e=248 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173682B2
Source datasetuspto-grants-2012_05
ORD IDord-48245b33302c4981af23248b9263243b
Source noteuspto-grants-2012_05