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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245230Generated: November 1, 2026

Ceric ammonium nitrate → N-[3-(5.6-Dimethoxy-3-methyl-1,4-benzoquinon-2-yl)methyl-2-(4-pyridyl)benzoyl]piperidine

https://huagongshe.com/reaction/1245230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCeric ammonium nitrateHCID 180504—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[3-(3,4,5,6-Tetramethoxy-2-methylbenzyl)-2-(4-pyridyl)benzoyl]piperidineHCID 21919137—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-[3-(5.6-Dimethoxy-3-methyl-1,4-benzoquinon-2-yl)methyl-2-(4-pyridyl)benzoyl]piperidineHCID 2191916546%

Reaction Steps

N-[3-(3,4,5,6-Tetramethoxy-2-methylbenzyl)-2-(4-pyridyl)benzoyl]piperidine (74 mg, 0.1510 mmol) was dissolved in a mixed solvent of acetonitrile (9 ml) and water (3 ml), then CAN (206 mg, 0.3759 mmol) was added thereto at room temperature and the mixture was stirred for 1 hour. The reaction solution was poured into water, neutralized with a saturated aqueous solution of sodium hydrogen carbonate and extracted with ethyl acetate. The extract was washed with water and dried and the solvent was evaporated therefrom. The residue was purified by preparative thin layer silica gel (hexane:ethyl acetate=1:5) to give the title compound (32 mg, 0.0695 mmol, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122543B2
Source datasetuspto-grants-2006_10
ORD IDord-3a977edc3b374ee294f8d238aec4b9ad
Source noteuspto-grants-2006_10