HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenylbenzyl chloride → (4-Phenylbenzyl)trichlorosilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylbenzyl chloride | HCID 15463 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (4-Phenylbenzyl)trichlorosilane | HCID 23264907 | 85% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.22 g (0.75 mmol) of tetrabutylphosphonium chloride, 1.52 g (7.5 mmol) of 4-phenylbenzyl chloride, 10 ml of dried benzene, and 3.05 g (22.5 mmol) of trichlorosilane were reacted at 150° C. for 2 hrs. The resulting mixture was distilled to give 1.70 g of (4-phenylbenzyl)trichlorosilane (yield; 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392077B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-91411a28b3f743fabab029e7b962e076 |
| Source note | uspto-grants-2002_05 |