Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylbenzene | HCID 7500 | — |
| Reactant | m-Divinylbenzene | HCID 7941 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | p-Divinylbenzene | HCID 66041 | — |
| Reactant | 1,2-Diethenylbenzene | HCID 66666 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 53693694 | HCID 53693694 | — |
Reaction Steps
In 100 ml of cyclohexane was dissolved 65.0 g of divinylbenzene (a 55% ethylbenzene solution of a mixture of m-divinylbenzene and p-divinylbenzene) and after adding dropwise thereto an amine-amide complex composed of 64.5 g of di-n-butylamine and 25 mmoles of n-butyl lithium, the mixture was heated to 50° C. for 3 hours. To the reaction mixture was added 1 ml of methanol. After concentrating the mixture, 1 g of di-tert-butylcatechol was added to the residue, and then the resultant mixture was distilled under reduced pressure to provide 53.5 g of (di-n-butylaminoethyl)styrene (a colorless liquid having a boiling point of 100.0°-101.0° C./1 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05015551 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-aa0881a3d14f430381a50d0db628f9de |
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| Source note | uspto-grants-1991_05 |
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