HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 962375Erstellt: 25. Oktober 2026
Maleic Anhydride → p-Butoxystyrene maleic anhydride
https://huagongshe.com/reaction/962375
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | p-Butoxystyrene | HCID 11715272 | — |
| Edukt | t-Butylperoxy(2-ethylhexanoate) | HCID 22065482 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | p-Butoxystyrene maleic anhydride | HCID 86752682 | 70% |
Reaktionsschritte
In an autoclave equipped with a 1.5-liter glass polymerization vessel and purged with nitrogen, polymerization reaction was carried out by dissolving 125.0 grams (0.71 mol) of p-butoxystyrene and 125.0 grams (1.28 mol) of maleic anhydride in 500 grams of acetone, adding 7.5 grams of t-butylperoxy(2-ethylhexanoate) as a polymerization catalyst, and heating the mixture at 90° C. Thereafter, the catalyst was added in incremental amounts, that is, 5.0 grams after 21/2 hours and 2.5 grams after 41/2 hours from the start of polymerization reaction. After 6 hours of polymerization, the reaction solution was cooled down and the acetone was distilled off. A 9/1 methanol/water mixture was added to the reaction solution, causing the copolymer to crystallize. The copolymer had a weight average molecular weight (Mw) of 9,600, a dispersity (Mw/Mn) of 1.58, and a copolymerization ratio of 6:7. The yield was 70.0%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05759739 |
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| Quelldatensatz | uspto-grants-1998_06 |
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| ORD ID | ord-1f83f2d28cdb454cb4075c13574d9f7f |
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| Quellennotiz | uspto-grants-1998_06 |
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