Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Methylbuta-1,3-diene;styrene | HCID 159989 | — |
Reaction Steps
700 grams of cyclohexane containing 100 ppm of tetrahydrofuran and 18 g of styrene monomer were charged to a reactor of 2 litres of capacity, of stainless steel, equipped with thermostatting jacket and stirring system. The mixture was heated up to 50° C. and then 0.09 g of n-butyl-lithium in solution in n-hexane was added to it. After 25 minutes of reaction, the temperature had increased up to 55° C. A sample was collected in order to check the reaction mixture for the complete conversion of the monomer into polymer and measure the molecular weight, then 72 g of isoprene was added and the polymerization was allowed to proceed during 20 minutes; after that time period, the second monomer was completely converted. The temperature of the mixture resulted to be of approximately 90° C. Thus, a living diblock styrene-isoprene (S-I) polymer was obtained, which was then submitted to coupling in order to form a three-arm radial polymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668208 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-a2dd9f23c2a247e587d21eca2b826c62 |
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| Source note | uspto-grants-1997_09 |
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