HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-Chloroethyl)benzene → Trichloro(diphenylmethyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-Chloroethyl)benzene | HCID 12648 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Product | Trichloro(diphenylmethyl)silane | HCID 15822893 | 43.8% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.14 g (0.47 mmol) of tetrabutylphosphonium chloride, 0.95 g (4.69 mmol) of 1-chloroethylbenzene, and 1.91 g (14.10 mmol) of trichlorosilane were reacted at 150° C. for 6 hrs. The resulting mixture was distilled to give 0.31 g diphenyl-1-trichlorosilylmethane (yield; 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392077B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-65fa92cc0a74401b950c164ccf6346fe |
| Source note | uspto-grants-2002_05 |