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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexane-1,2-dicarboxylic acid bis(oxiranylmethyl) ester | HCID 21660 | — |
| Reactant | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Bis[2-hydroxy-3-(4-hydroxy-2,2,6,6-tetramethylpiperidino)propyl]1,2-cyclohexanedicarboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04371644 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-ee22b69748ff4768a121917b54e2e5a7 |
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| Source note | uspto-grants-1983_02 |
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