HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092311Generated: November 3, 2026
Chloroacetone → Cyclopropyl-5-methyl-1,3-dihydro-imidazol-2-one
https://huagongshe.com/reaction/1092311
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Cyclopropyl-5-methyl-1,3-dihydro-imidazol-2-one | HCID 55300021 | 35.2% |
Reaction Steps
Chloroacetone (2.0 g), potassium cyanate (1.84 g) and cyclopropylamine (6.17 g) were dissolved or suspended in DMF (25 mL) and heated to 50° C. over night. The appearance of the suspension changed and on the second day a fine precipitate was observed. The suspension was concentrated in vacuo and the residue was treated with 25% HCl (25 mL) and DCM (50 mL) for one hour with vigorous stirring. The layers were separated and the organic phase was washed with brine, dried over Na2SO4 and evaporated. The residue was purified by flash chromatography using a gradient of methanol in ethyl acetate (0 to 5%) as an eluent to give 1-cyclopropyl-5-methyl-1,3-dihydro-imidazol-2-one as colorless solid (1.05 g). 1H-NMR (δ, CDCl3): 9.80 (br s, 1H), 5.79 (d, J=1.2 Hz, 1H), 2.91 (m, 1H), 2.012 (d, J=1.2 Hz, 3H), 0.92-0.84 (m, 2H), 0.82-0.77 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129423B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-f714a0da80f74e89926c7330a040aed3 |
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| Source note | uspto-grants-2012_03 |
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