HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl chloride → Trichloro-2-propen-1-ylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Product | Trichloro-2-propen-1-ylsilane | HCID 7867 | 20% |
| Product | Propyltrichlorosilane | HCID 8850 | 20% |
| Product | 1,3-Bis(trichlorosilyl)propane | HCID 11243856 | 17% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.037 g (0.14 mmol) of triphenylphosphine, 1.4 mg (0.014 mmol) of CuCl, 1.07 g (14.0 mmol) of allyl chloride, and 9.48 g (70.0 mmol) of trichlorosilane were reacted at 150° C. for 10 hrs. The resulting mixture was distilled to give 0.5 g of allytrichlorosilane (bp; 117-8° C., yield; 20%), 0.51 g of propyltrichlorosilane (bp; 123-5° C., yield; 20%), and 0.73 g of 1,3-bis(trichlorosilyl)propane (bp; 88-90° C./12.5 mmHg, yield; 17%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251057B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-2eea8f0e151d477caf73a5c824033852 |
| Source note | uspto-grants-2001_06 |