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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262057Generated: October 25, 2026

Ammonium cerium-nitrate → (S)-(+)-5-(3,4-dihydroxy-3-methyl-1-butyl)-2,3,6-trimethyl-p-benzoquinone

https://huagongshe.com/reaction/262057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium cerium-nitrateHCID 57418452—
Reactant(S)-4-(3,5-dimethoxy-3,4,6-trimethyl-phenylethyl)-2,2,4-trimethyl-1,3-dioxolanHCID 70593036—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(S)-(+)-5-(3,4-dihydroxy-3-methyl-1-butyl)-2,3,6-trimethyl-p-benzoquinoneHCID 1310053641.4%

Reaction Steps

While stirring for 2 minutes at room temperature, 2.01 g of cerium ammonium nitrate in 7.5 ml of water were added dropwise to a solution of 550 mg of (S)-4-(3,5-dimethoxy-3,4,6-trimethyl-phenylethyl)-2,2,4-trimethyl-1,3-dioxolan in 7.5 ml of acetonitrile. After 2 minutes of additional stirring, the reaction mixture was extracted three times with 20 ml of chloroform each time. The combined organic extracts were dried over sodium sulfate, whereafter the solvent was removed. After chromatography of the obtained residue on silica gel with benzene/ethyl acetate (2:1 parts by volume) and ethyl acetate, there were obtained 266 mg of (S)-(+)-2,3,6-trimethyl-5-(2,2,4-trimethyl-1,3-dioxolan-4-ethyl)-p-benzoquinone and 177 mg of (S)-(+)-5-(3,4-dihydroxy-3-methyl-1-butyl)-2,3,6-trimethyl-p-benzoquinone in the form of yellow needles with a melting point of 111°-112°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04153614
Source datasetuspto-grants-1979_05
ORD IDord-cda46522b62f43ce85fa6f88c66430e4
Source noteuspto-grants-1979_05