HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353092Generated: October 25, 2026
Sodium Iodide → 4-(3,5-Dimethylbenzyl)-3,5-heptanedione
https://huagongshe.com/reaction/353092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,5-Heptanedione | HCID 81923 | — |
| Reactant | 3,5-Dimethylbenzyl bromide | HCID 141334 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 4-(3,5-Dimethylbenzyl)-3,5-heptanedione | HCID 21877090 | 44.2% |
Reaction Steps
A solution of 3,5-heptanedione (1.24 ml, 9.13 mmol) in 2-butanone (40 ml) was treated with sodium hydride (60% dispersion in oil) (402 mg, 10.05 mmol) (added in portions) and stirred at room temperature for 10 minutes. Sodium iodide (1.5 g, 10.05 mmol) and then by 3,5-dimethylbenzyl bromide (2.0 g, 10.05 mmol) were added to the reaction mixture which was stirred at room temperature for 18 hours. The solution was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with water (×3). The organic phase was dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. The crude product was purified by flash chromatography on silica gel eluting with cyclohexane followed by cyclohexane:ethyl acetate (40:1, by volume) to afford the title compound as a yellow oil (995 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750230B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-ab3a1917d80c43939eecc3561cd7ad4e |
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| Source note | uspto-grants-2004_06 |
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