HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(bromomethyl)-N-(1,1-dimethylethyl)-1,1-dimethylsilanamine → 1-Tertbutylamino-2-(1-indenyl)-1,1-dimethylsilaethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(bromomethyl)-N-(1,1-dimethylethyl)-1,1-dimethylsilanamine | HCID 18000044 | — |
| Reactant | HCID 178506815 | HCID 178506815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Tertbutylamino-2-(1-indenyl)-1,1-dimethylsilaethane | HCID 18008512 | 29% |
Reaction Steps
A 20 g (182 mmol) solution of indenyl lithium in tetrahydrofurane was added to a solution of 41 g (182 mmol) of 2-bromo-1-tertbutylamino-1,1-dimethylsilaethane at 0° C. After the reaction was concentrated to dryness and the residue was extracted with hexane. Finally, the solution in hexane was concentrated to the obtainment of an orange oil: 13.5 g (52 mmol, yield: 29%). 1H-NMR (CDCl3): 7.50(m,1H), 7.39(m,1H), 7.35(m,1H), 7.23(m,1H), 6.17(m,1H), 3.42(m,2H), 2.17(m,2H), 1.22(m,9H), 0.20(m,6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06635778B1 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-1f078a4c580d4f2db7160e336e1727bd |
| Source note | uspto-grants-2003_10 |