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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
Reactant3,5-HeptanedioneHCID 81923—
Reactant3,5-Dimethylbenzyl bromideHCID 141334—
SolventMethyl Ethyl KetoneHCID 6569—
Product4-(3,5-Dimethylbenzyl)-3,5-heptanedioneHCID 2187709044.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750230B2
Source datasetuspto-grants-2004_06
ORD IDord-ab3a1917d80c43939eecc3561cd7ad4e
Source noteuspto-grants-2004_06