HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → Benzene, [(trichlorosilyl)methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Product | Benzene, [(trichlorosilyl)methyl]- | HCID 69863 | 96% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.15 g (0.75 mmol) of tri-n-butylphosphine, 0.95 g (7.5 mmol) of benzyl chloride, and 5.08 g (37.5 mmol) of trichlorosilane were reacted at 150° C. for 2 hrs. The resulting mixture was distilled to give 1.6 g of benzyltrichlorosilane (bp; 140-2° C./10 mmHg, yield; 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251057B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-32430181204e4c4584c1a4843efea0d2 |
| Source note | uspto-grants-2001_06 |