HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane → (2-Dimethylamino-4,5-dimethylcyclopentadienyl)(2-allyloxy-3-tert-butyl-5-methylphenyl)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane | HCID 21880918 | — |
| Reactant | HCID 178506779 | HCID 178506779 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Dimethylamino-4,5-dimethylcyclopentadienyl)(2-allyloxy-3-tert-butyl-5-methylphenyl)dimethylsilane | HCID 58747148 | 102.7% |
Reaction Steps
A solution of (2-allyloxy-3-tert-butyl-5-methylphenyl)dimethylchlorosilane (7.0 mmol) in toluene (12.1 mL) was added dropwise to a solution of 1-dimethylamino-3,4-dimethylcyclopentadienyllithium (7.0 mmol) in tetrahydrofuran (10.5 mL) and the mixture was stirred at room temperature for 6 hours. After the solvent was distilled off under reduced pressure, dehydrated pentane was added and a precipitated solid was filtered off. The filtrate was concentrated to obtain the title compound (2.86 g, 100%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241927B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-a04a230a05d749bfa956d26fb244d585 |
| Source note | uspto-grants-2007_07 |