HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dichloropropane → 1,3-Bis(trichlorosilyl)propane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dichloropropane | HCID 8881 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Product | Trichloro(3-chloropropyl)silane | HCID 75693 | 14% |
| Product | 1,3-Bis(trichlorosilyl)propane | HCID 11243856 | 72% |
Reaction Steps
In the same apparatus and procedure as Example 1 above, 0.44 g (1.50 mmol) of tetrabutylphosphonium chloride, 0.85 g (7.5 mmol) of 1,3-dichloropropane, and 10.16 g (75.0 mmol) of trichlorosilane were reacted at 150° C. for 10 hrs. The resulting mixture was distilled to give 1.68 g of 1,3-bis(trichlorosilyl)propane (yield; 72%) and 0.22 g of (3-chloropropyl)trichlorosilane (yield; 14%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392077B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-4e600918000f4c37a1bb05bb1f3d518f |
| Source note | uspto-grants-2002_05 |