HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959484Generated: October 30, 2026
Styrene → Benzene, ethenyl-, polymer with 1,3-butadiene
https://huagongshe.com/reaction/1959484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | 2-Propyl tetrahydrofurane | HCID 551240 | — |
| Reactant | HCID 86620807 | HCID 86620807 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Benzene, ethenyl-, polymer with 1,3-butadiene | HCID 62697 | — |
Reaction Steps
To a 10 oz. nitrogen purged bottle, hexane (20 mL), styrene (1 gr, 30% in hexane), butadiene (5 gr, 20% in hexane), oligomeric oxolanyl propane (OOPs) (0.03 mL, 1.6M solution) and butyl lithium (0.1 mL, 1.54M) would be added. The bottle would be placed into 80° C. water bath for 10 minutes. After cooling to 23° C., a charge of cinnamyl-1-methylpyrene ether (10 mL, 0.14M in cyclohexane) would be added into the bottle. After continual cooling for 5 minutes, a charge of DVB (0.5 mL) would be added to the mixture. The reaction would proceed for 1 hour, and then would be terminated by adding isopropanol 0.1 mL).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410225B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-edcf516085b0469db1f2e5614c4442ef |
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| Source note | uspto-grants-2013_04 |
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