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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616584Generated: October 25, 2026

Sodium hydride → HCID 20367917, compound

https://huagongshe.com/reaction/616584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,5-Dimethylhexane 2,5-dihydroperoxideHCID 520470—
Reactant1-t-Butylazo-1-chlorocyclohexaneHCID 23344784—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20367917HCID 2036791780%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a cooled slurry of 2.47 grams (.0586 moles) of 57% sodium hydride in 80 ml. of dioxane in a 250 ml. 4 neck round bottom flask equipped with a magnetic stirrer, thermometer, addition fummel and gas outlet, was slowly added 3.88 grams (0.0196 moles) of 90% 2,5-dimethyl-2,5-dihydroperoxy-hexane containing 8% water. After the addition was complete the reaction was stirred for 4 hours at 30° C, cooled to 15° C in a cold water bath and 7.96 grams (.0392 moles) of 1-t-butylazo-1-chlorocyclohexane was added dropwise holding the temperature at 15° to 20° C. After the addition was complete the reaction was stirred for 30 minutes at 15° to 20° C and poured into 200 ml. of ice cold water. The product was extracted with 50 ml. of cold pentane, the pentane solution washed with ice cold water, saturated NaHCO3 solution, dried over anhydrous sodium sulfate, filtered and the pentane evaporated under reduced pressure while holding the temperature of the solution below 10° C. The product was a light yellow liquid weighing 8.0 grams (80% yield). The infrared spectrum of the crude azo-peroxide was in agreement with the stucture of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04075199
Source datasetuspto-grants-1978_02
ORD IDord-8092dffe0eee4708bd965514e5159ba3
Source noteuspto-grants-1978_02