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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537671Generated: October 29, 2026

Sodium Iodide → HCID 49765294, compound

https://huagongshe.com/reaction/537671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHexamethyldisilazaneHCID 13838—
Reactant(1R,2R)-N1,N1-Dimethylcyclohexane-1,2-diamineHCID 11275066—
ReactantHCID 49765293HCID 49765293—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 49765294HCID 49765294—

Reaction Conditions

Temperature180 °C

Reaction Steps

To a mixture of 2-(5-bromo-2-ethylphenyl)cyclohexane-1,3-dione (0.917 g, 3.11 mmol), sodium iodide (0.934 g, 6.23 mmol) and hexamethyldisilazane (0.454 g, 3.11 mmol) is added copper (I) iodide (0.030 g, 0.15 mmol) and trans-N,N-dimethyl-1,2-cyclohexane diamine (0.044 g, 0.31 mmol). Degassed dioxane (5 ml) is added and the mixture is purged with nitrogen then heated at 180° C. for 1 hour under microwave irradiation. After cooling to room temperature the reaction mixture is treated with 2M aqueous hydrochloric acid and extracted with dichloromethane. The phases are separated and the aqueous phase is further extracted with dichloromethane. Organic fractions are combined then evaporated under reduced pressure to yield a crude product which is purified by flash column chromatography (10% ethyl acetate/hexane to 70% ethyl acetate/hexane eluant) to afford 2-(2-ethyl-5-iodophenyl)cyclohexane-1,3-dione as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865623B2
Source datasetuspto-grants-2014_10
ORD IDord-87d2f789a9394e3680500b84f128f3e8
Source noteuspto-grants-2014_10