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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 443761Erstellt: 25. Oktober 2026

Cyanuric chloride → 3-(4,6-Dichloro-s-triazin-2-yl)-3-azabicyclo[3.2.2]nonane

https://huagongshe.com/reaction/443761

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanuric chlorideHCID 7954—
Edukt3-Azabicyclo[3.2.2]nonaneHCID 9240—
EduktSodium HydroxideHCID 14798—
EduktAcetone cardiceHCID 18522661—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt3-(4,6-Dichloro-s-triazin-2-yl)-3-azabicyclo[3.2.2]nonaneHCID 15572579—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

Two hundred and eighty grams (1.5 mole) of cyanuric chloride is dissolved in 1.4 l. of acetone, then 1.8 l. of water is added and the mixture cooled to -10° C. using a dry-ice/acetone bath. 130 g. (1.0 mole) of 3-azabicyclo[3.2.2]nonane slurried in 200 ml. of acetone is then added all at once and the reaction is allowed to stir at -10° C. for 15 minutes. 100 ml. of 10 N NaOH is then added all at once giving rise to a small exotherm. After cooling to -10° C. using the dry-ice/acetone bath, the reaction mixture is stirred without further cooling for 3.8 hours allowing the temperature to rise to about 20° C. Two liters of water is then added, the precipitate filtered off and then washed with water. The precipitate is then dissolved in chloroform, excess water separated, the chloroform solution dried over magnesium sulfate and filtered through Magnesol®. The Magnesol® is then washed with chloroform, solvent removed in vacuo and recrystallized from dichloromethane-hexanes giving 170 g. of needles, m.p. 153°-154° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04261892
Quelldatensatzuspto-grants-1981_04
ORD IDord-2075d1d3da21407ebaecfa4f04bc37d2
Quellennotizuspto-grants-1981_04