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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24384Generated: October 25, 2026

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

https://huagongshe.com/reaction/24384

Reaction equation

Participants

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

Reaction Steps

5-Acetyl-2-oxindole (2 g) and 15 ml of trifluoroacetic acid in an ice bath was slowly treated with 1.8 g of triethylsilane and then stirred at room temperature for 5 hours. One ml of triethylsilane was added and 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 5-ethyl-2-oxindole as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855730B2
Source datasetuspto-grants-2005_02
ORD IDord-c8e3e385743e4295901d90ded8b42ade
Source noteuspto-grants-2005_02