Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Styrene-butadiene-styrene | HCID 22280236 | — |
Reaction Steps
In a 5 l jacketed autoclave equipped with a stirrer were charged 1667 g of cyclohexane, 12.1 mmol of sec-butyl lithium, and 4.5 mmol of N,N,N',N'-tetramethylethylene-diamine, and 250 g of a 30 wt % cyclohexane solution of styrene was added thereto. Polymerization was carried out at 75° C. To the reaction system, a 30 wt % cyclohexane solution of 1167 g of 1,3-butadiene and 250 g of a 30 wt % cyclohexane solution of styrene were added thereto, and polymerization was continued to obtain an SBS (styrene-butadiene-styrene) terblock copolymer. Two percent of the sec-butyl lithium was deactivated with a trace water content, leaving 11.9 mmol of active lithium. To the resulting living polymer solution was added 12.37 mmol of ethanol to deactivate the polymer terminals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05886108 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-acb806f601b7479a8742fe3d83797aeb |
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| Source note | uspto-grants-1999_03 |
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