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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | 2-Bromo-1-cyclopropylpropan-1-one | HCID 45080805 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-cyclopropyl-5-methyl-1H-imidazole | HCID 58035646 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440665B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-18e3b12ab877461bbbb124345669ba42 |
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| Source note | uspto-grants-2013_05 |
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