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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72265Generated: October 27, 2026

Sodium Iodide → 3-(2-Ethyl-5-iodophenyl)bicyclo[3.2.1]octane-2,4-dione

https://huagongshe.com/reaction/72265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHexamethyldisilazaneHCID 13838—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Reactant3-(5-Bromo-2-ethylphenyl)bicyclo[3.2.1]octane-2,4-dioneHCID 66679569—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product3-(2-Ethyl-5-iodophenyl)bicyclo[3.2.1]octane-2,4-dioneHCID 68485600100%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a microwave vial is added 3-(5-bromo-2-ethylphenyl)bicyclo[3.2.1]octane-2,4-dione (1.00 g, 3.11 mmol), sodium iodide (0.93 g, 6.23 mmol), hexamethyldisilazane (0.45 g, 3.11 mmol), copper(I) iodide (0.03, 0.15 mmol), trans-N,N′-dimethylcyclohexane-1,2-diamine (0.044 g, 0.31 mmol) then degassed dioxane (5 ml). After purging with nitrogen the mixture is heated at 180° C. for 1 hour under microwave irradiation. The mixture is cooled to room temperature, quenched with 2M hydrochloric acid and extracted with dichloromethane (×2). Organic fractions are combined, washed with saturated aqueous sodium metabisulfite, dried over magnesium sulfate then filtered. The filtrate is concentrated in vacuo, then purified by flash column chromatography (20% to 100% ethyl acetate/hexane eluant ratio) to afford 3-(2-ethyl-5-iodophenyl)bicyclo[3.2.1]-octane-2,4-dione (1.14 g, 100%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828908B2
Source datasetuspto-grants-2014_09
ORD IDord-584597383866409495d5bd2f8b801da4
Source noteuspto-grants-2014_09