Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoprene | HCID 6557 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Styrene | HCID 7501 | — |
| Product | HCID 19842620 | HCID 19842620 | — |
Reaction Steps
In a pressure vessel where dry nitrogen had been substituted, styrene was polymerized at 60° C. in cyclohexane as a solvent in the presence of s-butyllithium as a polymerization initiator, and then TMEDA was added as a Lewis base. Then, isoprene and styrene were consecutively polymerized to give a styrene-isoprene-styrene block copolymer. The thus-obtained block copolymer was hydrogenated in cyclohexane in the presence of Pd/C as a catalyst under a 2 MPa hydrogen atmosphere, to give a hydrogenated block copolymer (the hydrogenated block copolymer obtained in Referential Example 2 will be abbreviated as “Copolymer No. 1” hereinafter). Table 3 shows a styrene content, a number average molecular weight, a vinyl bond content and a hydrogenation ratio of the obtained Copolymer No. 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06977105B1 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-e7f8d6354c674b08a7acfba0ec169268 |
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| Source note | uspto-grants-2005_12 |
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