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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478190Generated: October 26, 2026

Methyl iodide → 5-Acetyl-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrile

https://huagongshe.com/reaction/478190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Cyclohexyl-3-oxopropanenitrileHCID 11309597—
ReactantDmf CS2HCID 86590990—
Product5-Acetyl-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrileHCID 22019043—

Reaction Steps

To a solution of 3-cyclohexyl-3-oxo-propionitrile in DMF:CS2 (1:1) was added K2CO3 at 0° C. and the reaction mixture stirred at ambient temperature for 2 hours. To the resulting reaction mixture was added chloroacetone (1 equivalent) and the reaction mixture stirred at ambient temperature for 3 hours. Iodomethane was then added and the resulting mixture was stirred at ambient temperature overnight. The reaction mixture was partitioned between ethyl acetate and brine, the organic phase dried with MgSO4 and the solvent was removed under reduced pressure. The crude product was purified by silica gel chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642227B2
Source datasetuspto-grants-2003_11
ORD IDord-29d6a6c76aba42dd88801346e36fbcae
Source noteuspto-grants-2003_11