HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456841Generated: October 30, 2026
Sodium Chloride → 2,4-Bis[(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-6-chloro-s-triazine
https://huagongshe.com/reaction/1456841
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | 2-chloro-4,6-bis[N-(2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-s-triazine | HCID 19073316 | — |
| Catalyst | Molybdenum trioxide | HCID 14802 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 2,4-Bis[(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-6-chloro-s-triazine | HCID 22507638 | 74% |
Reaction Steps
A mixture of 57.7 g (0.448 mol) of 70% aqueous tert-butylhydroperoxide, 250 ml of cyclohexane and 100 ml of saturated sodium chloride solution is agitated vigorously and the organic layer is then separated and dried over anhydrous magnesium sulfate. The drying agent is removed by filtration. The filtrate, 30.0 g (0.056 mol) of 2-chloro-4,6-bis[N-(2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-s-triazine and 1.0 g of molybdenum trioxide are placed in a pressure bottle and heated at 130°-140° C. The reaction mixture quickly turns red and heating is continued till the red color is discharged. The reaction mixture is allowed to cool and solids are removed by filtration. The filtrate is concentrated under reduced pressure to give an oil which is purified by flash chromatography on silica gel to afford 30.3 g. (74% yield) of the title compound as a white glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05844026 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-0e2e04efba8e4a5cb0ca8a00885788bc |
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| Source note | uspto-grants-1998_12 |
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