HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1,1,1,3,3-Pentachloro-1,3-disilabutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | Dichloro(chloromethyl)methylsilane | HCID 73788 | — |
| Product | 1,1,1,3,3-Pentachloro-1,3-disilabutane | HCID 12608648 | 58% |
| Product | Dichloro[(dichlorosilyl)methyl]methylsilane | HCID 15646422 | 14% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.20 g (0.75 mmol) of triphenylphosphine, 1.07 g (7.5 mmol) of (chloromethyl)methyldichlorosilane, and 5.08 g (37.5 mmol) of trichlorosilane were reacted at 150° C. for 24 hrs. The resulting mixture was distilled to give 1.0 g of 1,1,1,3,3-pentachloro-1,3-disilabutane (bp; 181-182° C., yield; 58%) and 0.1 g of 1,1,3,3-tetrachloro-1,3-disilabutane (bp; 166-167° C., yield; 14%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251057B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-4d44f5c2ed9040daace6d9f7a6f88ec9 |
| Source note | uspto-grants-2001_06 |