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HRID 2073464Erstellt: 24. Oktober 2026

1H-Pyrrole-2,5-dione, 1,1'-(4-methyl-1,3-phenylene)bis- → 4-[o-(1-Propenyl)phenoxy]benzophenone

https://huagongshe.com/de/reaction/2073464

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-Pyrrole-2,5-dione, 1,1'-(4-methyl-1,3-phenylene)bis-HCID 80893—
Edukt1,1'-(Methylenedi-p-phenylene)bismaleimideHCID 83648—
Eduktm-AminobenzohydrazideHCID 84178—
EduktLactateHCID 91435—
Edukt1H-Pyrrole-2,5-dione, 1,1'-(2,2,4-trimethyl-1,6-hexanediyl)bis-HCID 170261—
Produkt4-[o-(1-Propenyl)phenoxy]benzophenoneHCID 54415597—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

m-Aminobenzoic acid hydrazide (4 parts) is blended with methylglycolate and heated to 60° C. to obtain a solution. A mixture of 4,4'-bismaleimidodiphenylmethane (70 parts), 2,4-bismaleimidotoluene (30 parts) and 1,6-bismaleimido(2,2,4-trimethyl)hexane (2 parts) and methylglycolate was added and the mixture heated to 120° C. to give a homogeneous solution. The solvent was stripped off to give a molten BMI resin to which 66 parts of the product of Example 12 was added and melt blended. The homogeneous melt was degassed in vacuum, cast into a parallel epipedic mould and cured for 2 hours at 170° C., plus 4 hours at 210° C., at a pressure of 4 bars. After demoulding, the casting is post-cured for 5 hours at 240° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04917954
Quelldatensatzuspto-grants-1990_04
ORD IDord-742b82aabb8b493e892a654eebdedb31
Quellennotizuspto-grants-1990_04