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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | 3-(5-Bromo-2-ethylphenyl)bicyclo[3.2.1]octane-2,4-dione | HCID 66679569 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(2-Ethyl-5-iodophenyl)bicyclo[3.2.1]octane-2,4-dione | HCID 68485600 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828908B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-584597383866409495d5bd2f8b801da4 |
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| Source note | uspto-grants-2014_09 |
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