HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414151Erstellt: 24. Oktober 2026
2,2,4-Trimethylhexane → 4-[o-(1-Propenyl)phenoxy]benzophenone
https://huagongshe.com/de/reaction/414151
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,2,4-Trimethylhexane | HCID 28022 | — |
| Edukt | 1H-Pyrrole-2,5-dione, 1,1'-(4-methyl-1,3-phenylene)bis- | HCID 80893 | — |
| Edukt | 1,1'-(Methylenedi-p-phenylene)bismaleimide | HCID 83648 | — |
| Edukt | m-Aminobenzohydrazide | HCID 84178 | — |
| Edukt | Lactate | HCID 91435 | — |
| Produkt | 4-[o-(1-Propenyl)phenoxy]benzophenone | HCID 54415597 | — |
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-trimethylhexane (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 60 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04789704 |
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| Quelldatensatz | uspto-grants-1988_12 |
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| ORD ID | ord-472a124bbcc0464ebbea5b2271ba92f0 |
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| Quellennotiz | uspto-grants-1988_12 |
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