Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 616584Erstellt: 25. Oktober 2026

Sodium hydride → HCID 20367917, Verbindung

https://huagongshe.com/reaction/616584

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt2,5-Dimethylhexane 2,5-dihydroperoxideHCID 520470—
Edukt1-t-Butylazo-1-chlorocyclohexaneHCID 23344784—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 20367917HCID 2036791780%

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04075199
Quelldatensatzuspto-grants-1978_02
ORD IDord-8092dffe0eee4708bd965514e5159ba3
Quellennotizuspto-grants-1978_02