HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 5-Ethyl-1,3-dihydro-2H-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 5-acetyl-2,3-dihydro-1H-indol-2-one | HCID 10219643 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-Ethyl-1,3-dihydro-2H-indol-2-one | HCID 10154189 | 71% |
Reaction Steps
To 5-Acetyl-2-oxindole (2 g) in 15 mL of trifluoroacetic acid in an ice bath was slowly added 1.8 g of triethylsilane; the reaction was then stirred at room temperature for 5 hours. One mL of triethylsilane was added and the stirring continued overnight. The reaction mixture was poured into ice water and the resulting precipitate collected by vacuum filtration, washed copiously with water and dried under vacuum to give 1.3 g (71% yield) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130238 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-58f53a85daa748e2b07683f6b72dff20 |
| Source note | uspto-grants-2000_10 |