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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723616Generated: October 25, 2026

Sodium Iodide → 4-(3,5-Dimethylbenzyl)-3,5-heptanedione

https://huagongshe.com/reaction/723616

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 numberUS07141585B2
Source datasetuspto-grants-2006_11
ORD IDord-5e1d81a15bc24f788783e2a8a269c717
Source noteuspto-grants-2006_11