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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254542Generated: October 25, 2026

Potassium Iodide → 4-(1-benzyl-1H-imidazol-2-ylmethyl)-heptane-3,5-dione

https://huagongshe.com/reaction/254542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3,5-HeptanedioneHCID 81923—
Reactant1-benzyl-2-(chloromethyl)-1H-imidazoleHCID 736792—
ReactantSodium ethoxideHCID 2723922—
Reactant1-benzyl-2-(chloromethyl)-1H-imidazole hydrochlorideHCID 2779243—
SolventEthanolHCID 702—
Product4-(1-benzyl-1H-imidazol-2-ylmethyl)-heptane-3,5-dioneHCID 5895186131.5%

Reaction Steps

To a solution of 1.74 ml (4.7 mmol; ˜21% solution in ethanol) sodium ethanolate in 18 ml dry ethanol were added 600 mg (4.7 mmol) 3,5-heptanedione and stirred at ambient temperature for 30 min. Then a solution of 1-benzyl-2-chloromethyl-1H-imidazole (prepared from 1.081 g (4.5 mmol) 1-benzyl-2-chloromethyl-1H-imidazole hydrochloride in 7 ml ethanol and 1.74 ml (5 mmol; ˜21% solution in ethanol) sodium ethanolate) was added together with 30 mg potassium iodide. The mixture was heated to 50° C. for 10 min and then immediately cooled to ambient temperature and concentrated under reduced pressure at max. 30° C. Purification by flash-chromatography on silica gel with heptane/ethyl acetate 1:1 as eluent provided 423 mg 4-(1-benzyl-1H-imidazol-2-ylmethyl)-heptane-3,5-dione as light brown oil: MS (ISP): 299.2 ((M+H)+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875645B2
Source datasetuspto-grants-2011_01
ORD IDord-f45ec7e7b62747a79a67191e786acfef
Source noteuspto-grants-2011_01