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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478178Generated: October 25, 2026

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

https://huagongshe.com/reaction/478178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Methylphenyl)-3-oxopropanenitrileHCID 522513—
SolventDimethylformamideHCID 6228—
Product5-Acetyl-2-methylsulfanyl-4-(4-methyl-phenyl)-thiophene-3-carbonitrileHCID 22019029—

Reaction Steps

3-(4-Methyl-phenyl)-3-oxo-propionitrile (5 mmol) was added to a suspension of K2CO3 (3 equivalents, 15 mmol) in DMF (4.5 mL) and allowed to stir at room temperature. After 10 minutes, CS2 (1.25 equivalents, 7.5 mmol) was added in one portion and the resulting mixture stirred at room temperature for an additional 10 minutes. A solution of 1-chloro-propan-2-one (1.0 equivalent, 5 mmol) in DMF (5 mL) was added. After 1 hour, a solution of MeI (1.1 equivalents, 5.5 mmol) in DMF (2 mL) was added in a dropwise fashion. After 30 minutes, the mixture was poured onto water and the resulting mixture was stirred vigorously for 12-16 hours to afford a suspension of the desired product. The crude product was isolated by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642227B2
Source datasetuspto-grants-2003_11
ORD IDord-44f98405d5d643d3857ebadae006d0e6
Source noteuspto-grants-2003_11