HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 1,1,1,3,4-Pentachloro-3-methyl-1,3-disilabutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Silane, chlorodimethyl[(trichlorosilyl)methyl]- | HCID 11010110 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1,1,1,3,4-Pentachloro-3-methyl-1,3-disilabutane | HCID 19745090 | — |
Reaction Steps
A stirrer was added to a 250 ml, round bottomed flask, which was equipped with a bubbling column linked to a dry ice/aceton condenser and a chlorine gas cylinder. To the flask were added 100 g (0.41 mole) of 1,1,1,3-tetrachloro-3-methyl-1,3-disilabutane and 1 g of a reaction initiator, azobisisobutyronitrile, using carbon tetrachloride as a solvent. The obtained mixture was photoreacted for 5 hrs using a sun lamp, while bubbling chlorine gas and refluxing carbon tetrachloride. After confirming the degree of the reaction process by gas chromatography, the reaction mixture was distilled under vacuum to obtain 38 g of 1,1,1,3,4-pentachloro-3-methyl-1,3-disilabutane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05235061 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-5f896affc5fb491b8b9a0583e5b85969 |
| Source note | uspto-grants-1993_08 |