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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742478Generated: November 1, 2026

5-[4-(2,4,5-Trimethyl-3,6-dimethoxyphenoxy)benzyl]thiazolidine-2,4-dione → 5-[4-(3,5,6-Trimethyl-1,4-benzoquinon-2-yloxy)benzyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/1742478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[4-(2,4,5-Trimethyl-3,6-dimethoxyphenoxy)benzyl]thiazolidine-2,4-dioneHCID 19009243—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-[4-(3,5,6-Trimethyl-1,4-benzoquinon-2-yloxy)benzyl]thiazolidine-2,4-dioneHCID 1523051570.3%

Reaction Steps

A solution of 2.1 g of ceric ammonium nitrate in a mixture of 2 ml of water and 2 ml of acetonitrile was added dropwise at 0° C. to a solution of 0.4 g of 5-[4-(2,4,5-trimethyl-3,6-dimethoxyphenoxy)benzyl]thiazolidine-2,4-dione (prepared as described in Preparation 2) in 3 ml of acetonitrile, and the resulting mixture was stirred at the same temperature for 1 hour. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate. The solvent was then removed from the extract by distillation under reduced pressure, and the residue thus obtained was purified by column chromatography through silica gel, using a 4:1 by volume mixture of benzene and ethyl acetate as the eluent, to give 260 mg of the title compound, melting at 153°-156° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338855
Source datasetuspto-grants-1994_08
ORD IDord-169b3c1446aa42d58668b1020d7a0db3
Source noteuspto-grants-1994_08