Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240849Generated: October 30, 2026

Hydrogen Peroxide → 2,2-Dimethyl-3-phenyl-cyclopropanecarboxylic acid amide

https://huagongshe.com/reaction/2240849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2-Dimethyl-3-phenylcyclopropanecarbonitrileHCID 13429898—
SolventDimethyl SulfoxideHCID 679—
SolventSodium chloride; waterHCID 57417360—
Product2,2-Dimethyl-3-phenyl-cyclopropanecarboxylic acid amideHCID 57652787—

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium carbonate (467 mg) was added to a solution of 2,2-dimethyl-3-phenyl-cyclopropanecarbonitrile (3/1 cis/trans mixture, 4 g, 23.4 mmol) in DMSO (7 mL). The resulting mixture was cooled to 0° C. and an aqueous solution of hydrogen peroxide (30%, 2.8 mL) was added. The reaction mixture was allowed to warm up to room temperature and was stirred overnight. A second aliquot of aqueous solution of hydrogen peroxide (30%, 2.8 mL) was added and the resulting mixture was stirred for 24 hours. A third aliquot of aqueous solution of hydrogen peroxide (30%, 3.0 mL) was added and the resulting mixture was stirred for 3 days. The reaction mixture was poured into brine and extracted with ethyl ether. The organic layer was separated, dried over Na2SO4, filtered, and evaporated under reduced pressure. The crude residue was purified by flash chromatography (0% to 65% of EtOAc in hexane) to give 2.66 of 2,2-dimethyl-3-phenyl-cyclopropanecarboxylic acid amide (2/1 trans/cis mixture), together with 1.125 g of starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723391B2
Source datasetuspto-grants-2010_05
ORD IDord-a84b4d5c25714a378f072e7ac14052ee
Source noteuspto-grants-2010_05