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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758188Generated: October 27, 2026

Cyclohexane-1,2-dicarboxylic acid bis(oxiranylmethyl) ester → Bis[2-hydroxy-3-(4-hydroxy-2,2,6,6-tetramethylpiperidino)propyl]1,2-cyclohexanedicarboxylate

https://huagongshe.com/reaction/1758188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexane-1,2-dicarboxylic acid bis(oxiranylmethyl) esterHCID 21660—
Reactant4-Hydroxy-2,2,6,6-tetramethylpiperidineHCID 75471—
SolventBenzeneHCID 241—
ProductBis[2-hydroxy-3-(4-hydroxy-2,2,6,6-tetramethylpiperidino)propyl]1,2-cyclohexanedicarboxylateHCID 86738787—

Reaction Steps

A mixture of 11.0 g of 4-hydroxy-2,2,6,6-tetramethylpiperidine and 7.0 g of bis(2,3-epoxypropyl)1,2-cyclohexanedicarboxylate was heated, with stirring, at 170°-180° C. for 5 hours. After completion of the reaction, benzene was added to the reaction mixture and then the benzene solution was washed with water and dried over anhydrous potassium carbonate. The solvent was evaporated under reduced pressure from the benzene solution, leaving a residue, which was then purified by column chromatography through silica gel eluted with a 16:2:1:1 by volume mixture of ethyl acetate, benzene, ethanol and triethylamine, giving the desired Compound No. 90 as a vitreous solid. The Compound had an Rf value of 0.32 on thin-layer chromatography on silica gel developed with a 16:2:3:1 by volume mixture of ethyl acetate, benzene, ethanol and triethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371644
Source datasetuspto-grants-1983_02
ORD IDord-ee22b69748ff4768a121917b54e2e5a7
Source noteuspto-grants-1983_02