Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Styrene | HCID 7501 | — |
| Edukt | Methylcyclohexane | HCID 7962 | — |
| Edukt | 2-Methylpyridine | HCID 7975 | — |
| Edukt | Isobutylene | HCID 8255 | — |
| Edukt | (1-Chloro-1-methylethyl)benzene | HCID 70281 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Butyl Chloride | HCID 8005 | — |
| Produkt | Isobutylene styrene | HCID 44154101 | — |
Reaktionsschritte
Into a 2 L reaction container having an agitator, 589 mL of methylcyclohexane (dried with molecular sieves), 613 ml of n-butyl chloride (dried with molecular sieves), and 0.550 g of cumyl chloride were added. The reaction container was cooled to −70° C., and then 0.35 mL of α-picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization. They were reacted with each other for 2.0 hours while stirring the solution at −70° C. Next, 59 mL of styrene was added to the reaction container, and reaction was continued for another 60 minutes. Thereafter, a large amount of methanol was added to stop the reaction. After removing a solvent and the like from the reaction solution, the polymer was dissolved with toluene and rinsed twice. This toluene solution was added to a methanol mixture to precipitate a polymer. The polymer thus obtained was dried at 60° C. for 24 hours, thereby obtaining a styrene-isobutylene diblock copolymer.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09346227B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-33458a051763415d9db0f0a2940d31aa |
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| Quellennotiz | uspto-grants-2016_05 |
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