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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224735Generated: 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/224735

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 numberUS04234490
Source datasetuspto-grants-1980_11
ORD IDord-12f2e00f35a244c6bc18dd4018a4c9b1
Source noteuspto-grants-1980_11