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HRID 345990Erstellt: 24. Oktober 2026

Cyanuric chloride → 2,4-Dichloro-6-(4,4-ethylenedioxy-2,2,6,6-tetramethylpiperidin-1yl)-1,3,5-triazine

https://huagongshe.com/de/reaction/345990

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanuric chlorideHCID 7954—
Edukt7,7,9,9-Tetramethyl-1,4-dioxa-8-azaspiro[4.5]decaneHCID 567045—
LösungsmittelO-XyleneHCID 7237—
Produkt2,4-Dichloro-6-(4,4-ethylenedioxy-2,2,6,6-tetramethylpiperidin-1yl)-1,3,5-triazineHCID 19991770—

Reaktionsschritte

A solution of 55.3 g (0.3 mol) of cyanuric chloride in 300 ml of xylene is added dropwise with stirring and cooling to 0°-5° to a solution of 119.6 g (0.6 mol) of 4,4-ethylenedioxy-2,2,6,6-tetramethylpiperidine in 100 ml of xylene. The mixture is subsequently heated to reflux and kept at boiling point for 26 hours. After addition of 150 ml of xylene, the mixture is allowed to cool and the precipitate is filtered off. The filtrate is evaporated in vacuo. The residue is recrystallized from 300 ml of acetonitrile. The product obtained is a brownish powder which melts at 169°-172°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05059689
Quelldatensatzuspto-grants-1991_10
ORD IDord-c7bb789d0b1d4f4bacfa19354d6ade46
Quellennotizuspto-grants-1991_10