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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactanttert-Butyl hydroperoxideHCID 6410—
Reactant2-chloro-4,6-bis[N-(2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-s-triazineHCID 19073316—
CatalystMolybdenum trioxideHCID 14802—
SolventCyclohexaneHCID 8078—
Product2,4-Bis[(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-6-chloro-s-triazineHCID 2250763874%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05844026
Source datasetuspto-grants-1998_12
ORD IDord-0e2e04efba8e4a5cb0ca8a00885788bc
Source noteuspto-grants-1998_12