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 | Styrene-butadiene-styrene | HCID 22280236 | — |
Reaction Steps
In a 2 gallon autoclave reactor, 4,500 g of cyclohexane was charged, followed by 9 g of tetrahydrofuran, 112.5 g of styrene monomer and 1.7 g of n-butyllithium. This mixture was subjected to polymerization for 1 hr. Then, 525 g of 1,3-butadiene monomer was added in the reactor and polymerization was carried out for 1 hr. Thereafter, 112.5 g of styrene monomer was charged and subjected to further polymerization for 1 hr, to give a styrene-butadiene-styrene block copolymer with a number average molecular weight of about 40,000 in which the styrene bond amounted to 30.4% (block styrene content 29.9%) while the 1,2-vinyl bond content of the butadiene unit amounted to 40.5%. 2.5 mmol of living lithium was found to be contained in per 100 g of the polymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05994477 |
|---|
| Source dataset | uspto-grants-1999_11 |
|---|
| ORD ID | ord-d5cf9ee140b64a4084f036e37bc4cd60 |
|---|
| Source note | uspto-grants-1999_11 |
|---|