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HRID 128366Erstellt: 27. Oktober 2026

Dibutylamine → Dibenzo[d,f][1,3,2]dioxaphosphepin-6-amine, N,N-dibutyl-2,4,8,10-tetrakis(1,1-dimethylethyl)-

https://huagongshe.com/reaction/128366

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibutylamineHCID 8148—
EduktTriethylamineHCID 8471—
EduktPhosphorus trichlorideHCID 24387—
Edukt3,3',5,5'-Tetrakis(1,1-dimethylethyl)(1,1'-biphenyl)-2,2'-diolHCID 80808—
LösungsmittelTolueneHCID 1140—
ProduktDibenzo[d,f][1,3,2]dioxaphosphepin-6-amine, N,N-dibutyl-2,4,8,10-tetrakis(1,1-dimethylethyl)-HCID 20481433—

Reaktionsschritte

170 g (0.414 mol) of 4,4',6,6'-tetra-tert-butyl-2,2'-biphenol in 150 ml of toluene is heated to 80°-90° C. in a nitrogen atmosphere, and 40 ml (0.458 mol) of phosphorus trichloride is added dropwise in the course of 2 hours. The reaction mixture is stirred at reflux temperature for 4 hours and, towards the end of the reaction, nitrogen gas is again introduced. There is then added dropwise at reflux temperature, during 11/2 hours, a solution of 53.5 g (0.414 mol) of dibutylamine and 41.9 g (0.414 mol) of triethylamine in 80 ml of toluene. After 15 hours, the reaction mixture is allowed to cool to room temperature, and the triethylamine hydrochloride which has precipitated is filtered off. The toluene is afterwards evaporated off, and the N-(2,4,8,10-tetra-tert-butyl-dibenz[d,f][1,3,2]dioxaphosphepin-6-yl)-dibutylamine obtained has a melting point of 140° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04259492
Quelldatensatzuspto-grants-1981_03
ORD IDord-79a7db922a534ba2add9c61c300cfdb6
Quellennotizuspto-grants-1981_03