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 | HCID 19842620 | HCID 19842620 | — |
Reaction Steps
In a pressure-resistant container replaced with dry nitrogen, styrene was polymerized at 60° C. using cyclohexane as a solvent and s-butyllithium as a polymerization initiator, TMEDA was added thereto as a Lewis base, and thereafter isoprene and styrene were successively polymerized thereto to give a styrene-isoprene-styrene block copolymer. The resulting block copolymer was hydrogenated in cyclohexane under a hydrogen atmosphere at a hydrogen pressure of 2 MPa using Pd/C as a catalyst, to give a hydrogenated block copolymer (the hydrogenated block copolymer obtained in Preparation Example 4 being hereinafter simply referred to as a block copolymer 4). The content of styrene, the number-average molecular weight, the content of vinyl bonds and the hydrogenation rate of the resulting block copolymer 4 are shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07147905B2 |
|---|
| Source dataset | uspto-grants-2006_12 |
|---|
| ORD ID | ord-b8baf13fabc74010a4ef6b10a29d71d9 |
|---|
| Source note | uspto-grants-2006_12 |
|---|