HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichlorodimethylsilane → Bis(indeno[1,2-b]indolyl)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichlorodimethylsilane | HCID 6398 | — |
| Reactant | (4-Methylphenyl)hydrazine | HCID 10875 | — |
| Reactant | 6-Methyl-1-indanone | HCID 2795093 | — |
| Reactant | HCID 178420856 | HCID 178420856 | — |
| Product | Bis(indeno[1,2-b]indolyl)dimethylsilane | HCID 22597295 | — |
Reaction Steps
Consider the preparation of the N-G-N linked complex 6, below. An indenoindole compound is first prepared by reacting 6-methyl-1-indanone and p-tolylhydrazine. Deprotonation of the indenoindole at nitrogen, followed by reaction with 0.5 eq. of dichlorodimethylsilane gives a bis(indeno[1,2-b]indolyl)dimethylsilane (5). This neutral compound is doubly deprotonated and then reacted with 2 eq. of cyclopentadienyl-zirconium trichloride to give the desired bimetallic complex, 6. A similar approach is used to generate phenylboranyl complex 8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06841500B2 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-22f12ff164a745048f2d8d0a9c57df46 |
| Source note | uspto-grants-2005_01 |