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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690855Generated: October 31, 2026

Iodoethane → HCID 66707577, compound

https://huagongshe.com/reaction/1690855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl cyclohex-3-en-1-ylcarbamateHCID 11063381—
ReactantCyclohexane ethylacetateHCID 21867204—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 66707577HCID 6670757758%

Reaction Steps

To a solution of cyclohex-3-enyl-carbamic acid tert-butyl ester (Kampferer, P.; Vasella, A. Helvetica Chimica Acta 2004, 87, 2764-2789) (4.34 g, 22 mmol) in 20 ml of DMSO was added sodium hydride (880 mg, 60% dispersion, 22 mmol) and after one hour of stirring ethyl iodide (1.78 ml, 22 mmol). After further stirring for 2 hours at room temperature the reaction mixture was concentrated under reduced pressure. The residue was diluted with water and brine and extracted three times with ethyl acetate. The organic layers were dried over sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and after chromatography (silica, cyclohexane/ethyl acetate=12/1) the title compound (Rf=0.30, 2.88 g, 58% yield) was obtained as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153689B2
Source datasetuspto-grants-2012_04
ORD IDord-56b4ab63a7b241e488769b2fbdc4c686
Source noteuspto-grants-2012_04