Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Methylcyclohexane | HCID 7962 | — |
| Reactant | 2-Methylpyridine | HCID 7975 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | (1-Chloro-1-methylethyl)benzene | HCID 70281 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Butyl Chloride | HCID 8005 | — |
| Product | Isobutylene styrene | HCID 44154101 | — |
Reaction Steps
Methylcyclohexane (dried with molecular sieves) of 589 mL, n-butyl chloride (dried with molecular sieves) of 613 mL, and cumyl chloride of 0.550 g were added to a 2 L reaction container having an agitator. After cooling the reaction container to −70° C., α-picoline (2-methylpyridine) of 0.35 mL and isobutylene of 179 mL were added. Titanium tetrachloride of 9.4 mL was further added, and the polymerization was stared. The solution was agitated at −70° C. and allowed to react for 2.0 hours. Next, styrene of 59 mL was added to the reaction container, and the reaction was continued for 60 minutes. After that, a large amount of methanol was added to stop the reaction. After a solvent and the like were removed from the reaction solution, the polymer was dissolved in toluene and washed twice. The toluene solution was added to a methanol mixture to deposit the polymer, and the obtained polymer was dried at 60° C. for 24 hours to obtain a styrene-isobutylene diblock copolymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09259969B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-87527eaccbca4443b490e5c7bedd1d20 |
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| Source note | uspto-grants-2016_02 |
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