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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939738Generated: October 30, 2026

Ammonium cerium (IV) nitrate → 1,4-Naphthalenedione, 2-(1-hydroxypentyl)-5,8-dimethoxy-

https://huagongshe.com/reaction/1939738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium cerium (IV) nitrateHCID 9869224—
ReactantHCID 21468091HCID 21468091—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1,4-Naphthalenedione, 2-(1-hydroxypentyl)-5,8-dimethoxy-HCID 1051860148%

Reaction Steps

3.6 g (10.3 mmole) of 2-(1-hydroxyhexyl)-1,4,5,8-tetramethoxynaphthalene was dissolved in 50 ml of acetonitrile and then a solution of 14.2 g (25.0 mmole) of cerium (IV) ammonium nitrate dissolved in 50 ml of distilled water was added dropwise thereto over 30 minutes through a dropping funnel in a cooling bath (0°-5° C.). The reaction mixture was stirred at normal temperature for 2 hours. After adding 100 ml of distilled water thereto, the reaction mixture was extracted twice with dichloromethane solvent, dried over anhydrous magnesium sulfate and then filtered through filter paper. The resulting filtrate was concentrated under reduced pressure to obtain a crude product. The crude product was purified by silica gel column chromatography (silica gel 4.0×15 cm) using the solvent condition which increases the amount of ethylacetate so that the n-hexane/ethylacetate ratio can vary from 5:1 to 1:3, to obtain 1.2 g of the title compound as a yellow precipitate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696276
Source datasetuspto-grants-1997_12
ORD IDord-48a16014f2324ab9a81be88829277fc4
Source noteuspto-grants-1997_12