Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | M-Cresol | HCID 342 | — |
| Edukt | 3-Mercaptopropionic Acid | HCID 6514 | — |
| Edukt | Salicylaldehyde | HCID 6998 | — |
| Edukt | 2,6-Dimethylol-p-cresol | HCID 7039 | — |
| Edukt | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | m-Cresol-salicylaldehyde | HCID 86745981 | — |
Reaktionsschritte
A mixture of 146.0 g m-cresol, 25.2 g 2,6-bis(hydroxymethyl)-p-cresol, 5.0 g 3-mercaptopropionic acid and 1.5 g p-toluene-sulfonic acid monohydrate in 200 ml glacial acetic acid were charged into a 1-L reaction vessel equipped with a paddle stirrer, reflux condenser and a nitrogen inlet tube. The mixture was heated to reflux and maintained at reflux to allow formation of the alternating copolymer. After 8 hours, 146.5 g salicylaldehyde were added over time to the reaction mixture to form substantially m-cresol-salicylaldehyde block segments. Reflux was continued for 8 hours. The reaction mixture was slowly poured into 7 L deionized water to precipitate the resin. Once the solvent had exchanged with water, the product was collected on a filter, slurried once in warm deionized water for about 30 minutes, again collected, rinsed with water and dried in a vacuum oven under about 125 mm Hg and at about 100 to 105° C. About 281 g of a block copolymer resin having a number average molecular weight, Mn, of 1472 Daltons and a Tg of 233° C. were obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05419995 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-3a961eec5e2b42d9a9f3b2e594e0751d |
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| Quellennotiz | uspto-grants-1995_05 |
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