HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → Bis(2-methylpropyl)(phenoxy)alumane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Triisobutylaluminum | HCID 16682931 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Bis(2-methylpropyl)(phenoxy)alumane | HCID 16697999 | — |
Reaction Steps
In a manner analogous to that described in Example 1, triisobutylaluminum and phenol are reacted in absolute toluene to give phenoxy-diisobutylaluminum and this is then reacted with pyridine-N-oxide-2-thiol to give the title compound. The isolation of the product is carried out in an analogous manner. The yield of phenoxy-bis(2-pyridinethiolato)aluminum N,N'-dioxide, a white solid, is 98% of theory. Melting point: 240°-241° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04421749 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-fd7b380b926942f69a4859bb5c596a01 |
| Source note | uspto-grants-1983_12 |