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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091627Generated: November 1, 2026

Triethylamine → 4-cyclopropyl-5-methyl-1H-imidazole

https://huagongshe.com/reaction/2091627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantFormamidine acetateHCID 160693—
Reactant2-Bromo-1-cyclopropylpropan-1-oneHCID 45080805—
SolventEthanolHCID 702—
Product4-cyclopropyl-5-methyl-1H-imidazoleHCID 58035646—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Cyclopropyl-5-methyl-1H-imidazole was synthesized according to the following procedure: Under nitrogen with stirring formamidine acetate (15.62 g, 150 mmol) was suspended in 40 ml anhydrous ethanol. 2-bromo-1-cyclopropylpropan-1-one (2.64 g, 15 mmol) was added via syringe and the mixture was heated to 60° C. for 2 hours. Triethylamine (21 ml, 155 mmol) was then added and the reaction was heated for an additional 12 hours at 60° C. The solvent was removed under reduced pressure, and the residue was dissolved in 50 ml of water. An aqueous solution of saturated sodium bicarbonate (20 ml) was added, followed by sodium chloride until the solution became saturated. The mixture was placed in a separatory funnel and extracted with ethyl acetate (3×50 ml), the organic extracts combined, dried over magnesium sulfate, filtered and then the solvent removed under reduced pressure. The oily residue was washed with hexanes (2×100 ml) to remove any residual triethylamine, leaving an oily residue which was >90% pure by 1H-NMR, which was further purified by loading onto a silica gel column in ethyl acetate and eluting with 0 to 10% methanol in ethyl acetate. Yield 0.607 g, 33%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440665B2
Source datasetuspto-grants-2013_05
ORD IDord-18e3b12ab877461bbbb124345669ba42
Source noteuspto-grants-2013_05