HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-Chloroethyl)benzene → 1-Trichlorosilylethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-Chloroethyl)benzene | HCID 12648 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Product | 1-Trichlorosilylethylbenzene | HCID 11791289 | 35.4% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.20 g (0.68 mmol) of tetrabutylphosphonium chloride, 0.96 g (6.83 mmol) of 1-chloroethylbenzene, and 2.71 g (20.00 mmol) of trichlorosilane were reacted at 150° C. for 6 hrs. The resulting mixture was distilled to give 0.58 g 1-trichlorosilylethylbenzene (yield; 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392077B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-7a8a7685ee9849e8b6cf0805d69bd095 |
| Source note | uspto-grants-2002_05 |