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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6848Generated: October 26, 2026

Methyl iodide → 4-Acetyl-3-methyl-5-(methylthio)thiophene-2-carbonitrile

https://huagongshe.com/reaction/6848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
ReactantAcetylacetoneHCID 31261—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Acetyl-3-methyl-5-(methylthio)thiophene-2-carbonitrileHCID 2820186—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a slurry of 2,4-pentanedione (20 mmol) and K2CO3 (3 equivalents, 60 mmol) in DMF (10 mL) was added CS2 (1.2 equivalents, 24 mmol) and the resulting mixture stirred for 10 minutes. The mixture was cooled to 0° C. then chloroacetonitrile (1.0 equivalent, 20 mmol) was added and the reaction stirred 1 hour then warmed to room temperature and stirred for an additional 2 hours. The reaction mixture was again cooled to 0° C. and methyl iodide (1.05 equivalents, 22 mmol) was added slowly. The resulting mixture was warmed to room temperature. After 12 hours, water was added and the resulting suspension was stirred overnight. The desired product was isolated by filtration after washing with water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084159B2
Source datasetuspto-grants-2006_08
ORD IDord-fab1cf601eeb4f96bf3c58d1ce626549
Source noteuspto-grants-2006_08