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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358178Generated: October 30, 2026

Methyl iodide → HCID 178503864, compound

https://huagongshe.com/reaction/2358178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 22139854HCID 22139854—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178503864HCID 178503864—

Reaction Conditions

Temperature70 °C

Reaction Steps

1-(1,4-Dioxaspiro[4.5]dec-6-yl)-3-(4-methylthiophen-3-yl)thiourea (393 mg) was dissolved in absolute tetrahydrofuran (8.5 ml), and a solution of methyl iodide (179 mg) in absolute tetrahydrofuran (0.5 ml) was added. The mixture was then stirred at 70° C. in sand bath for 2 days. Ethyl acetate was then added to the reaction mixture, and the mixture was washed twice with water. The organic phase was dried over magnesium sulfate and the solvent was removed after filtration. The residue was purified by preparative chromatography and the product-containing fractions were combined, freed from acetonitrile, made basic and extracted three times with ethyl acetate. The organic phases were combined, dried (MgSO4) and filtered. This gave 59 mg of the desired product which was used directly for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763643B2
Source datasetuspto-grants-2010_07
ORD IDord-520929116c564d9d8bcec15e0820c7af
Source noteuspto-grants-2010_07