HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650031Generated: October 25, 2026
Sodium Chloride → Bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) succinate
https://huagongshe.com/reaction/1650031
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Bis(2,2,6,6-tetramethyl-4-piperidyl) succinate | HCID 93340 | — |
| Catalyst | Molybdenum trioxide | HCID 14802 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) succinate | HCID 21026400 | 137.6% |
Reaction Steps
A two-phase mixture of 70% aqueous t-butyl hydroperoxide (103.9 g, 807 mmol), cyclohexane (200 ml) and sodium chloride (15 g) is shaken in a separatory funnel. The organic phase is dried over magnesium sulfate, filtered, and added to 40.0 g (101 mmol) of di-(2,2,6,6-tetramethylpiperidin-4-yl) succinate. Molybdenum trioxide (2.0 g) is added, and the mixture is refluxed for one hour. Water is collected in a Dean-Stark trap. The entire reaction mixture is then transferred to a Fischer-Porter bottle and heated at 140° C. for 6 hours. Additional t-butyl hydroperoxide (90%, 10.1 g, 101 mmol) is added and heating is resumed for another 4 hours. The colorless reaction mixture is filtered, concentrated, and dissolved in heptane (200 ml). The heptane solution is passed through a short column of silica gel with heptane. Subsequent evaporation affords an oil which is crystallized from ethanol to yield 41.2 g (69%) of a white powder, m.p. 122°-6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921962 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-d3912e21d51f4a29badcf37cec627249 |
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| Source note | uspto-grants-1990_05 |
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