HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Trichlorophenol → HCID 20476806, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Trichlorophenol | HCID 6914 | — |
| Reactant | Triisobutylaluminum | HCID 16682931 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20476806 | HCID 20476806 | — |
Reaction Steps
In a manner analogous to that described in Example 1, 17.5 g of triisobutylaluminum and 17.4 g of 2,4,6-trichlorophenol are reacted in absolute toluene to give (2,4,6-trichlorophenoxy)diisobutylaluminum and this is then reacted with 22.4 g of pyridine-N-oxide-2-thiol to afford the title compound. The isolation of the product is carried out in analogous manner. The yield of (2,4,6-trichlorophenoxy)bis(2-pyridinethiolato)-aluminum N,N'-dioxide, a fine white powder with a melting point of 207°-208° C., is 28.6 g, about 68% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04421749 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-64daf94c4ca546a8afccf8766ddbde20 |
| Source note | uspto-grants-1983_12 |