HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-4-phenylindene → (2-Methyl-4-phenylindenyl)(t-butylamino)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-4-phenylindene | HCID 11074559 | — |
| Reactant | Dimethylsilyl(t-butylamino)chloride | HCID 123286153 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Methyl-4-phenylindenyl)(t-butylamino)dimethylsilane | HCID 19366102 | 82% |
Reaction Steps
2-methyl-4-phenylindene (synthesized substantially according to the technique reported in U.S. Pat. No. 5,329.033) (3.00 g, 0.014 moles) in THF (10 mL) was added dropwise to a stirring solution of KH (0.601 g, 0.0150 moles) in THF (50 mL). This mixture was allowed to stir for 16 hours. The solution was then filtered and added dropwise to a solution of dimethylsilyl(t-butylamino)chloride (2.41 g, 0.0145 moles) in THF (75 mL). This mixture was allowed to stir for 16 hours. After the reaction period the volatiles were removed and the residue extracted and filtered using hexane. Removal of the volatiles resulted in the isolation of the desired product as a light yellow oil (4.00 g, 82.0 percent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06015868 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-3ab94c12469443d7acbbcb2807abbccd |
| Source note | uspto-grants-2000_01 |