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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121551Generated: November 5, 2026

Triethylsilane → 5-Ethyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/2121551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactant5-acetyl-2,3-dihydro-1H-indol-2-oneHCID 10219643—
SolventTrifluoroacetic acidHCID 6422—
Product5-Ethyl-1,3-dihydro-2H-indol-2-oneHCID 1015418971%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696463B2
Source datasetuspto-grants-2004_02
ORD IDord-c3f7ea1d52294090b064e005287b6590
Source noteuspto-grants-2004_02