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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414116Erstellt: 25. Oktober 2026

Formaldehyde → Triethanolamine

https://huagongshe.com/reaction/414116

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktPhthalic AnhydrideHCID 6811—
Edukt2-Ethylhexyl acrylateHCID 7636—
Edukt2-EthylhexanolHCID 7720—
EduktEpichlorohydrinHCID 7835—
Edukt3-OctanolHCID 11527—
EduktPotassium HydroxideHCID 14797—
EduktN,N-Diethyl-1,3-propanediamineHCID 61011—
Edukt2-HydroxyputrescineHCID 164656—
Edukt1,3-OxazolidineHCID 536683—
KatalysatorTriethylamineHCID 8471—
Lösungsmittel1-Methoxy-2-propanolHCID 7900—
ProduktTriethanolamineHCID 7618—
ProduktDiisocyanatotolueneHCID 12905475—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

BM 2: 500 parts of an epoxy resin based on Bisphenol A and epichlorohydrin (epoxy equivalent weight about 500) are dissolved in 214 parts propyleneglycol monomethylether and reacted at 110° C. with 83 parts of a semiester of phthalic acid anhydride and 2 ethylhexanol, in the presence of 0.5 parts of triethylamine as catalyst, to an acid value of below 3 mg KOH/g. Then, 120 parts of an NH-functional oxazolidine of aminoethylethanolamine, 2-ethylhexylacrylate and formaldehyde, and 26 parts diethylaminopropylamine are added and the batch is reacted at 80° C. to an epoxy value of practically zero. The batch is diluted with 200 parts propyleneglycol monomethylether. 70 parts (resin solids) of this oxazolidine modified epoxy resin amine adduct are homogenized for 30 minutes at 50° C. with 30 parts based on resin solids of a crosslinking component obtained through reaction of 1 mole of a toluylene diisocyanate semi-blocked with 2-ethylhexanol and 0.33 moles triethanolamine. The reaction is carried out in a 70% solution of diethyleneglycol dimethylether, at 50 to 60° C. until all isocyanate groups have reacted.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04789696
Quelldatensatzuspto-grants-1988_12
ORD IDord-4a7f5ce4883543a39e6e73e605fb7938
Quellennotizuspto-grants-1988_12