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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6859Generated: October 26, 2026

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

https://huagongshe.com/reaction/6859

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 numberUS07084159B2
Source datasetuspto-grants-2006_08
ORD IDord-183102cc420b4877ac00ee09af6bc6a9
Source noteuspto-grants-2006_08