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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656213Generated: October 28, 2026

Iodoethane → HCID 66707577, compound

https://huagongshe.com/reaction/656213

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 numberUS08071643B2
Source datasetuspto-grants-2011_12
ORD IDord-2e0d7b6bc0bd4c45b9facaae5b8bb593
Source noteuspto-grants-2011_12