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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849500Generated: October 31, 2026

Hydrogen Peroxide → 4-(Adamantan-1-ylmethoxy)-3-(2-methoxypyridin-3-yl)benzamide

https://huagongshe.com/reaction/1849500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Adamantan-1-ylmethoxy)-3-(2-methoxypyridin-3-yl)benzonitrileHCID 86702844—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product4-(Adamantan-1-ylmethoxy)-3-(2-methoxypyridin-3-yl)benzamideHCID 8670284580.5%

Reaction Steps

To a solution of 4-(adamantan-1-ylmethoxy)-3-(2-methoxypyridin-3-yl)benzonitrile (1.15 g, 3.07 mmol) in dimethylsulfoxide (25 mL) and methylene chloride (25 mL) was added potassium carbonate (0.85 g, 6.15 mmol) followed by addition of 35% hydrogen peroxide aqueous solution (5.30 mL, 61.60 mmol) dropwise. The mixture was stirred at ambient temperature for 4 h, the volatiles were removed by evaporation in vacuo. The residue was diluted with water (100 mL). The precipitate was collected by filtration and washed with water to give the title compound as a colorless solid (0.97 g, 80%): 1H NMR (300 MHz, CDCl3) δ 8.18-8.15 (m, 1H), 7.84-7.79 (m, 1H), 7.71-7.69 (m, 1H), 7.54-7.50 (m, 1H), 6.95-6.91 (m, 2H), 5.85 (br s, 2H), 3.87 (s, 3H), 3.49 (s, 2H), 1.89 (br s, 3H), 1.68-1.37 (m, 12H); MS (ES+) m/z: 393.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-bc2812a0e26d4b83a615f725375b4b29
Source noteuspto-grants-2015_02