HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Di-tert-butylphenol → 2,4,6-Tri-tert-butylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Di-tert-butylphenol | HCID 7311 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Triethylaluminum | HCID 16682930 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,4,6-Tri-tert-butylphenol | HCID 12902 | — |
Reaction Steps
By the method used in Examples 1-33, 171 g (0.83 mol) 2,4-di-tert-butylphenol (2,4-DTBP) was dissolved in 350 ml hexane, and the amount (if any) of various polyhalophenols indicated in Table VI was added to the mixture, followed by addition of 5.8 mmol triethylaluminum to said mixture, at room temperature. The 2,4-DTBP was then reacted with 1.2-1.6 mol isobutene at 1.7 bar and 30° C., to form 2,4,6-tri-tert-butylphenol (2,4,6-TTBP).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292970 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-d7d07ec41dcb40d98d77f1bc90c4b85b |
| Source note | uspto-grants-1994_03 |