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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457642Generated: October 30, 2026

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

https://huagongshe.com/reaction/457642

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 numberUS07189721B2
Source datasetuspto-grants-2007_03
ORD IDord-65e8763664dd4b85896774c08921f2b6
Source noteuspto-grants-2007_03