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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51222Generated: October 27, 2026

Sulfuric Acid → HCID 178450295, compound

https://huagongshe.com/reaction/51222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418365HCID 178418365—
ReactantHCID 178510437HCID 178510437—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178450295HCID 17845029582%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713632B1
Source datasetuspto-grants-2004_03
ORD IDord-18f7f4b32dce4331b1fc18d695176e83
Source noteuspto-grants-2004_03