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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9299Generated: October 29, 2026

Hydrogen Peroxide → HCID 21986126, compound

https://huagongshe.com/reaction/9299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178419080HCID 178419080—
SolventEthanolHCID 702—
ProductHCID 21986126HCID 21986126—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of NiCl2 (0.364 g, 2.81 mmol) in EtOH (20 mL) was reacted with NaBH4 (0.053 mg, 1.40 mmol) at rt for 15 m after saturation of the solution with hydrogen gas. Ethylene diamine (0.17 g, 2.81 mmol) was added followed by the alkynyl imidazol (Intermediate R15, 0.26 g, 1.40 mmol) at rt for 45 m under an atmosphere of hydrogen gas. The mixture was filtered, diluted with chloroform and subjected to an aqueous work-up. The residue was purified by chromatography on SiO2 to give 4-(3-vinyl-cyclohex-3-enylmethyl)-1H-imidazole (72%). To 4-(3-vinyl-cyclohex-3-enylmethyl)-1H-imidazole (0.09 g, 0.47 mmol) in ethanol (3 mL) at 0° C. was added H2NNH2.H2O (0.93 mL, 19.1 mmol) followed by H2O2 (30%) (0.488 g, 14.4 mmol) and the mixture was stirred for 45 m at 0° C. and an additional 6 h at rt. The reaction was quenched and the material was purified by an aqueous work-up. The imidazole compound was purified further by isolation of the fumaric acid salt. The fumarate was converted to the compound 4-(3-ethyl-cyclohex-3-enylmethyl)-1,3-dihydro-imidazol-2-one (Compound 59) by the applicable step of Method P.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091232B2
Source datasetuspto-grants-2006_08
ORD IDord-694fed7805bc4205a8b843e02f34766d
Source noteuspto-grants-2006_08