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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428261Generated: October 28, 2026

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

https://huagongshe.com/reaction/428261

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 numberUS06313158B1
Source datasetuspto-grants-2001_11
ORD IDord-0732a96d41ab4475970b7fa108c2573f
Source noteuspto-grants-2001_11