HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Silane, trichloro[(trimethylsilyl)methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Product | Silane, trichloro[(trimethylsilyl)methyl]- | HCID 11816894 | 70% |
| Product | HCID 57370759 | HCID 57370759 | 7% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.20 g (0.75 mmol) of triphenylphosphine, 1.38 g (7.5 mmol) of (chloromethyl)trimethylsilane, and 5.08 g (37.5 mmol) of trichlorosilane were reacted at 150° C. for 10 hrs. The resulting mixture was distilled to give 1.2 g of 1,1,1,-trichloro-3,3-dimethyl-1,3-disilabutane (bp; 173-174° C., yield; 70%) and 0.1 g of 1,1-dichloro-3,3-dimethyl-1,3-disilabutane (bp; 157-159° C., yield; 7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251057B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-e4864bfb00c945da96b981a3089537cc |
| Source note | uspto-grants-2001_06 |