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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243386Generated: October 30, 2026

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

https://huagongshe.com/reaction/1243386

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 numberUS07119090B2
Source datasetuspto-grants-2006_10
ORD IDord-9a54d627849b480682aaae0bcace4d95
Source noteuspto-grants-2006_10