HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Bis(trichlorosilyl)methane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trichloro(chloromethyl)silane | HCID 15258 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Product | Bis(trichlorosilyl)methane | HCID 2756737 | 50% |
| Product | (Dichlorosilylmethyl)trichlorosilane | HCID 58212176 | 16% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.20 g (0.75 mmol) of triphenylphosphine, 0.92 g (7.5 mmol) of (chloromethyl)trichlorosilane, and 5.08 g (37.5 mmol) of trichlorosilane were reacted at 150° C. for 42 hrs. The resulting mixture was distilled to give 1.1 g of 1,1,1,3,3,3-hexachloro-1,3-disilapropane (bp; 173-174° C., yield; 50%) and 0.3 g of 1,1,1,3,3-pentachloro-1,3-disilapropane (bp; 166-167° C., yield; 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251057B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-9faab18ac8e0432fa3f36b96f922dcd9 |
| Source note | uspto-grants-2001_06 |