HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Silane, chlorodimethyl[(trichlorosilyl)methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | Silane, chloro(chloromethyl)dimethyl- | HCID 74393 | — |
| Product | Silane, chlorodimethyl[(trichlorosilyl)methyl]- | HCID 11010110 | 58% |
| Product | 1,1,3-Trichloro-3-methyl-1,3-disilabutane | HCID 15646421 | 8% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 1.0 g (3.8 mmol) of triphenylphosphine, 6.21 g (38.0 mmol) of (chloromethyl)dimethylchlorosilane, and 27.5 g (190.0 mmol) of trichlorosilane were reacted at 150° C. for 12 hrs. The resulting mixture was distilled to give 5.8 g of 1,1,1,3-tetrachloro-3-methyl-1,3-disilabutane (bp; 169-170° C., yield; 58%) and 1.2 g of 1,1,3-trichloro-3-methyl-1,3-disilabutane (bp; 153-155° C., yield; 8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251057B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-d4d3d7fcd7274167a56a3de17319aaeb |
| Source note | uspto-grants-2001_06 |