Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86741594 | HCID 86741594 | — |
Reaction Steps
In an autoclave were placed 4,000 g of cyclohexane, 100 g of 1,3-butadiene monomer, 0.53 g of n-butyllithium and tetrahydrofuran in a proportion of 40 moles per mole of n-butyllithium. They were subjected to polymerization for 30 minutes at 70° C., and then 150 g of styrene was added and subsequently polymerized for 60 minutes, after with 600 g of 1,3-butadiene was added and polymerized for 150 minutes. Thereafter, 150 g of styrene was added and subsequently polymerized for 60 minutes, to obtain a butadiene-styrene-butadiene-styrene block copolymer. The resulting living polymer solution was poured into a large amount of methanol for deactivation and precipitation. The precipitated polymer was vacuum-dried for 50 hours at 60° C. The polymer was a block copolymer having a bound styrene content of 30%, a block styrene content of 28% and a 1,2-vinyl content in the butadiene units of 35% (25% based on the weight of the entire copolymer) and having a number average molecular weight of about 120,000.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04673714 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-f82b11ec059942e4b04badbe64c980a0 |
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| Source note | uspto-grants-1987_06 |
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