HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chlorododecane → n-Butyl tri-n-dodecyltin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chlorododecane | HCID 8192 | — |
| Reactant | Butyltin trichloride | HCID 14236 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178443216 | HCID 178443216 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | n-Butyl tri-n-dodecyltin | HCID 20561756 | — |
Reaction Steps
The same reactor as used in Preparation Example 1 was charged with 12.1 g (0.5 mole) of magnesium, 102.4 g (0.5 mole) of n-dodecyl chloride and 200 g of tetrahydrofuran, and they were reacted in a stream of nitrogen. To the resulting n-dodecyl magnesium chloride solution was added dropwise a solution of 42.3 g (0.15 mole) of mono-n-butyltin trichloride in 200 ml of xylene with stirring at room temperature over the course of 30 minutes. Then, the reaction mixture was reacted for 3 hours at the refluxing temperature, and then subjected to a hydrolysis treatment to obtain 99.8 g of n-butyl tri-n-dodecyltin having a purity of 98.7% as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04301173 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-e56f7e1204bd45abb0b7387882979c92 |
| Source note | uspto-grants-1981_11 |