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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976418Generated: November 1, 2026

Methyl iodide → HCID 22644724, compound

https://huagongshe.com/reaction/1976418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22644783HCID 22644783—
SolventAcetoneHCID 180—
ProductHCID 22644724HCID 22644724—

Reaction Steps

A mixture of methyl 1-({[4-(2-butynyloxy)phenyl]sulfonyl}amino)cyclohexanecarboxylate (4.5 g.,12.3 mmol), anhydrous potassium carbonate (20.0 g, excess) and methyl iodide (2 g, 14.08 mmol) was refluxed in acetone for sixteen hours. The reaction mixture was then cooled to room temperature and filtered. The acetone layer was concentrated and extracted with chloroform. The chloroform layer was washed well with water, dried over anhydrous MgSO4, filtered and concentrated to provide methyl1-[{[4-(2-butynyloxy)phenyl]sulfonyl}(methyl)amino]cyclohexanecarboxylate as a yellow oil. Yield: 4.6 g(quantitative) Electrospray Mass Spec 380 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225311B1
Source datasetuspto-grants-2001_05
ORD IDord-7dbbe19433f64cb8ad1fd5c6edd751ad
Source noteuspto-grants-2001_05