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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030319Erstellt: 26. Oktober 2026

Dimethylamine → Tinuvin

https://huagongshe.com/reaction/1030319

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktTolueneHCID 1140—
Edukt2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxideHCID 14149470—
EduktHCID 178418361HCID 178418361—
KatalysatorHCID 178418390HCID 178418390—
Lösungsmittel1-ButanolHCID 263—
LösungsmittelWaterHCID 962—
ProduktTinuvinHCID 6253186,1%

Reaktionsschritte

33.2 g (0.1 mol) of 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole-N-oxide, 0.125 g of palladium carbon, 300 ml of a solvent mixture comprising toluene, butanol and water (ratio by volume of 1:1:1) and 5 g 50% dimethylamine were charged into a 500-ml stainless autoclave equipped with an agitator. After the air in the autoclave had been replaced by hydrogen, the pressure of hydrogen was set to 10 kg/cm2. The temperature of the resultant mixture was increased to 50° C. under agitation, and agitation was continued until no more hydrogen gas was absorbed by the mixture. The pressure of hydrogen was always kept at 8 to 10 kg/cm2 during the reaction. After the reaction had been completed, the autoclave was cooled, and the catalyst was filtered off. The most part of solvent was distilled off, and the residual solid was washed with isopropyl alcohol and then dried to obtain 27.2 g of 2-(2'-hydroxy-3'-t-butyl- 5'-methylphenyl)-5-chlorobenzotriazole as a target substance (yield, 86.2%; melting point, 138° to 140° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05104992
Quelldatensatzuspto-grants-1992_04
ORD IDord-24723d7b1a7641828cb4c0fff5e4aed4
Quellennotizuspto-grants-1992_04