HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Di-tert-butyl-4-methylphenol → Isobutylbis(2,6-di-tert-butyl-4-methylphenoxy)aluminum
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | Triisobutylaluminum | HCID 16682931 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | Isobutylbis(2,6-di-tert-butyl-4-methylphenoxy)aluminum | HCID 16688646 | — |
Reaction Steps
Using a 250 ml balloon flask disposed in an argon atmosphere and provided with a magnetic stirrer rod, a solution of 0.493 g of triisobutylaluminium in 20 ml of pentane is introduced, and then a solution of 1.095 g of 2,6-di-t-butyl-4-methylphenol in 30 ml of pentane is introduced dropwise with agitation and at ambient temperature. After about 30 hours of reaction the pentane is evaporated under vacuum and analysis of the white solid remaining indicates that it is formed essentially by bis-(2,6-di-t-butyl-4-methylphenoxy)-isobutylaluminium. That compound is put back into solution in 5 ml of heptane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05898092 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-a0b82ea0555541e3b42829d2da8cce29 |
| Source note | uspto-grants-1999_04 |