HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51222Generated: October 27, 2026
Sulfuric Acid → HCID 178450295, compound
https://huagongshe.com/reaction/51222
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178418365 | HCID 178418365 | — |
| Reactant | HCID 178510437 | HCID 178510437 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178450295 | HCID 178450295 | 82% |
Reaction Steps
A solution of 4-cyanoimidazole (42.7 g , 0.458 mol) in THF (500 ml) was added dropwise over 30 min to a solution (1.4 L, 1.47 mol, 3.2 equivalents) of 1.1 M isopropyl magnesium bromide in THF at 0 to 10° C. under a nitrogen atmosphere. The mixture was stirred at 15 to 25° C. for 3 h. Water (430 ml) and 10% aqueous sulfuric acid solution (860 ml) were successively added dropwise, and the mixture was stirred at 30 min. A 30% aqueous sodium hydroxide solution was added dropwise to adjust the pH to 8. After partitioning, the aqueous layer was extracted with ethyl acetate (300 ml×2). The organic layer was combined, and the mixture was washed successively with saturated aqueous sodium hydrogencarbonate and saturated brine, and concentrated under reduced pressure. The concentration residue was broken up with isopropyl ether (300 ml). The crystals were collected by filtration and washed with isopropyl ether. The crystals were dried in vacuo (40° C.) to give 1-(1H-imidazol-4-yl)-2-methyl-1-propanone (51.9 g, yield 82%). 1H-NMR (CDCl3): δ 1.25 (6H, d, J=6.9 Hz), 3.36 (1H, quint, J=6.9 Hz), 7.81 (1H, s), 7.87 (1H, s)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713632B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-18f7f4b32dce4331b1fc18d695176e83 |
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| Source note | uspto-grants-2004_03 |
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