HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → 3,3'-Bis(trimethylsiloxy)-4,4'-bis(trimethylsilylamino)biphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Dianisidine | HCID 8411 | — |
| Reactant | 3,3'-Dihydroxybenzidine | HCID 16918 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3,3'-Bis(trimethylsiloxy)-4,4'-bis(trimethylsilylamino)biphenyl | HCID 11156392 | — |
Reaction Steps
0.540 g 3,3'-dihydroxy-4,4'-diaminobiphenyl (synthesized from 3,3'-dimethoxy-4,4'-diaminobiphenyl using hydrogen iodide by the known method) and 1.52 g triethylamine were dissolved in 16 mL dry tetrahydrofuran. 1.63 g trimethylchlorosilane was then added dropwise followed by heating under reflux for 72 hours. Operating in an argon atmosphere, the salt was filtered off and the solvent, etc., was removed under reduced pressure to yield 3,3'-bis(trimethylsiloxy)-4,4'-bis(trimethylsilylamino)biphenyl. This monomer was prepared immediately prior to each of the polymerization reactions described below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464922 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-6d2ce9546d3c4c3f914f14bf20ede102 |
| Source note | uspto-grants-1995_11 |