HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium benzylamide → (Benzylamino)dimethyl(tetramethylcyclopentadienyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium benzylamide | HCID 10931395 | — |
| Reactant | (Tetramethylcyclopentadienyl)dimethylchlorosilane | HCID 131720376 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (Benzylamino)dimethyl(tetramethylcyclopentadienyl)silane | HCID 131720375 | — |
Reaction Steps
To a solution of 1.000 g (4.651 mmol) (chloro)(dimethyl)(tetramethylcyclopentadienyl)silane in 70 mL ether was slowly added 0.526 g (4.651 mmol) lithium benzylamide. The reaction mixture was stirred overnight, then the solvent was removed, the residue was extracted with pentane and filtered. The pentane was removed under reduced pressure to give the product as a pale yellow oil. The yield was 1.234 g (93.3%). Mass spec. m/e 285 (18%). 1H NMR (C6D6) δ 7.0-7.24 (m, 5H), 3.71 (d, 2H), 2.73 (br s, 1H), 1.88 (s, 6H), 1.76 (s, 6H), 0.43 (br t, 1H), −0.07 (s, 6H). 13C NMR (C6D6) δ 144.5, 135.7, 132.0, 128.5, 127.3, 126.7, 56.7, 46.4, 14.6, 11.4, −2.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06670432B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-4f2cf154348642579c56443cb103ae89 |
| Source note | uspto-grants-2003_12 |